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Links from MedGen

Items: 7

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NSMF
(P65H)
Single nucleotide variant
(missense variant)
Hypogonadotropic hypogonadism 9 with or without anosmia
GUncertain significance
NSMF
Microsatellite
(intron variant)
not provided
+1 more
GBenign/Likely benign
LOC126860797, NSMF
(R449G +4 more)
Single nucleotide variant
(missense variant)
Hypogonadotropic hypogonadism 9 with or without anosmia
GUncertain significance
NSMF
(R196C)
Single nucleotide variant
(missense variant)
Hypogonadotropic hypogonadism 9 with or without anosmia
GUncertain significance
LOC126860797, NSMF
(L421F +4 more)
Single nucleotide variant
(missense variant)
Hypogonadotropic hypogonadism 9 with or without anosmia
GUncertain significance
NSMF
Deletion
(intron variant)
Hypogonadotropic hypogonadism 9 with or without anosmia
Grisk factor
LOC126860797, NSMF
(T480A +4 more)
Single nucleotide variant
(missense variant)
Hypogonadotropic hypogonadism 9 with or without anosmia
Grisk factor
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