U.S. flag

An official website of the United States government

Format
Items per page
Sort by
Choose Destination

Search results

Items: 49

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ITGA7
Single nucleotide variant
(synonymous variant)
not specified
+2 more
GBenign/Likely benign
ITGA7
(T1003M +13 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
ITGA7
Single nucleotide variant
(intron variant)
not specified
+1 more
GBenign
ITGA7
Single nucleotide variant
(synonymous variant)
not specified
+1 more
GBenign/Likely benign
ITGA7
Single nucleotide variant
(intron variant)
not provided
+3 more
GBenign/Likely benign
ITGA7
Single nucleotide variant
(synonymous variant)
not specified
+2 more
GBenign
ITGA7
(I901V +13 more)
Single nucleotide variant
(missense variant)
not specified
+2 more
GBenign/Likely benign
ITGA7
(E882K +13 more)
Single nucleotide variant
(missense variant)
ITGA7-related condition
+3 more
GConflicting classifications of pathogenicity
ITGA7
(V881D +13 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
ITGA7
(G857S +13 more)
Single nucleotide variant
(missense variant)
ITGA7-related condition
+2 more
GConflicting classifications of pathogenicity
ITGA7, LOC126861535
Single nucleotide variant
(intron variant)
not provided
+1 more
GUncertain significance
ITGA7, LOC126861535
Single nucleotide variant
(intron variant)
not specified
+1 more
GBenign
ITGA7, LOC126861535
Single nucleotide variant
(intron variant)
not provided
+1 more
GConflicting classifications of pathogenicity
LOC126861535, ITGA7
Single nucleotide variant
(synonymous variant)
not specified
+2 more
GConflicting classifications of pathogenicity
ITGA7, LOC126861535
(I765V +13 more)
Single nucleotide variant
(missense variant)
not specified
+2 more
GConflicting classifications of pathogenicity
ITGA7, LOC126861535
(S696L +12 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
ITGA7, LOC126861535
(L679M +12 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
ITGA7, LOC126861535
Single nucleotide variant
(intron variant)
not specified
+2 more
GBenign
ITGA7
Single nucleotide variant
(synonymous variant)
not specified
+1 more
GBenign
ITGA7
(R651H +12 more)
Single nucleotide variant
(missense variant)
not specified
+1 more
GBenign
ITGA7
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
ITGA7
(G610R +12 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GBenign/Likely benign
ITGA7
(V591M +12 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
ITGA7
(I589L +12 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
ITGA7
Single nucleotide variant
(synonymous variant)
not provided
+2 more
GConflicting classifications of pathogenicity
ITGA7
Single nucleotide variant
(synonymous variant)
not provided
+2 more
GBenign/Likely benign
ITGA7
(L536F +12 more)
Single nucleotide variant
(missense variant)
ITGA7-related condition
+2 more
GConflicting classifications of pathogenicity
ITGA7
(A530V +12 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
ITGA7
Single nucleotide variant
(intron variant)
not provided
+1 more
GConflicting classifications of pathogenicity
ITGA7
Deletion
(intron variant)
not specified
+3 more
GBenign/Likely benign
ITGA7
Single nucleotide variant
(intron variant +1 more)
not provided
+1 more
GConflicting classifications of pathogenicity
ITGA7
Single nucleotide variant
(intron variant)
not specified
+1 more
GBenign
ITGA7
Single nucleotide variant
(synonymous variant +1 more)
ITGA7-related condition
+2 more
GBenign/Likely benign
ITGA7
Single nucleotide variant
(intron variant)
ITGA7-related condition
+3 more
GBenign
ITGA7
(R298C +7 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GUncertain significance
ITGA7
Single nucleotide variant
(synonymous variant +1 more)
not provided
+2 more
GBenign/Likely benign
ITGA7
(R275H +7 more)
Single nucleotide variant
(missense variant +1 more)
not specified
+1 more
GBenign
ITGA7
Single nucleotide variant
(synonymous variant +1 more)
not specified
+1 more
GBenign
ITGA7
Single nucleotide variant
(intron variant)
ITGA7-related condition
+3 more
GBenign/Likely benign
ITGA7
Single nucleotide variant
(synonymous variant +1 more)
not provided
GUncertain significance
ITGA7
Single nucleotide variant
(intron variant)
ITGA7-related condition
+3 more
GBenign/Likely benign
ITGA7
(T219I +3 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
ITGA7
Single nucleotide variant
(synonymous variant +2 more)
not provided
+1 more
GConflicting classifications of pathogenicity
ITGA7
(R173Q +2 more)
Single nucleotide variant
(missense variant +1 more)
Congenital muscular dystrophy due to integrin alpha-7 deficiency
+1 more
GUncertain significance
ITGA7
Single nucleotide variant
(intron variant)
not specified
+1 more
GBenign
ITGA7
Single nucleotide variant
(intron variant)
not specified
+1 more
GBenign
ITGA7
(L96W)
Single nucleotide variant
(missense variant +2 more)
Congenital muscular dystrophy due to integrin alpha-7 deficiency
+1 more
GUncertain significance
ITGA7
(P95L)
Single nucleotide variant
(missense variant +2 more)
Congenital muscular dystrophy due to integrin alpha-7 deficiency
+1 more
GUncertain significance
ITGA7
(R43L)
Single nucleotide variant
(missense variant +2 more)
not provided
+1 more
GUncertain significance
Format
Items per page
Sort by
Choose Destination