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rs797044965

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs797044965(A;A)
Make rs797044965(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position40818661
GeneKCNQ4
is asnp
is mentioned by
dbSNPrs797044965
ebirs797044965
HLIrs797044965
Exacrs797044965
Varsomers797044965
Maprs797044965
PheGenIrs797044965
hapmaprs797044965
1000 genomesrs797044965
hgdprs797044965
ensemblrs797044965
gopubmedrs797044965
geneviewrs797044965
scholarrs797044965
googlers797044965
pharmgkbrs797044965
gwascentralrs797044965
openSNPrs797044965
23andMers797044965
23andMe allrs797044965
SNP Nexus

SNPshotrs797044965
SNPdbers797044965
MSV3drs797044965
GWAS Ctlgrs797044965
Max Magnitude0
ClinVar
Risk rs797044965(A;A)
Alt rs797044965(A;A)
Reference rs797044965(T;T)
Significance Pathogenic
Disease DFNA 2 Nonsyndromic Hearing Loss
Variation info
Gene KCNQ4
CLNDBN DFNA 2 Nonsyndromic Hearing Loss
Reversed 0
HGVS NC_000001.10:g.41284333T>A
CLNSRC
CLNACC RCV000193083.1,