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Links from MedGen

Items: 2

VariationLocationGene(s)Protein changeCondition(s)Clinical significance
(Last reviewed)
Review status
1.
GRCh37:
Chr2:84899578
GRCh38:
Chr2:84672454
DNAH6D2194EAbnormal spermatogenesisUncertain significance
(Nov 1, 2019)
criteria provided, single submitter
2.
GRCh37:
Chr2:85023448
GRCh38:
Chr2:84796324
DNAH6G3753DAbnormal spermatogenesisUncertain significance
(Nov 1, 2019)
criteria provided, single submitter