RS398122997 GRHL2

Health Risk Chr 8:101644221
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What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal dominant nonsyndromic hearing loss 28
Autosomal dominant nonsyndromic hearing loss 28
Other Variants in GRHL2
rs2536962966 rs200745936 rs1811191593 rs140106332 rs776382416 rs2536814870 rs2536894997 rs372210965 rs2536859968 rs147703146
Ask Dr. Hemsworth about this variant