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rs886044309

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome8
Position101599152
GeneGRHL2
is asnp
is mentioned by
dbSNPrs886044309
dbSNP (classic)rs886044309
ClinGenrs886044309
ebirs886044309
HLIrs886044309
Exacrs886044309
Gnomadrs886044309
Varsomers886044309
LitVarrs886044309
Maprs886044309
PheGenIrs886044309
Biobankrs886044309
1000 genomesrs886044309
hgdprs886044309
ensemblrs886044309
geneviewrs886044309
scholarrs886044309
googlers886044309
pharmgkbrs886044309
gwascentralrs886044309
openSNPrs886044309
23andMers886044309
23andMe allrs886044309
SNPshotrs886044309
SNPdbers886044309
MSV3drs886044309
GWAS Ctlgrs886044309
Max Magnitude0
ClinVar
Risk rs886044309(A;A)
Alt rs886044309(A;A)
Reference Rs886044309(G;G)
Significance Probable-Pathogenic
Disease Deafness
Variation info
Gene GRHL2
CLNDBN Deafness, autosomal dominant 28
Reversed 0
HGVS NC_000008.10:g.102611380G>A
CLNSRC
CLNACC RCV000358123.1,