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rs797044966

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CTC;CTC) 0 common in clinvar
Make rs797044966(-;-)
Make rs797044966(-;CCT)
Make rs797044966(CCT;CCT)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position40819444
GeneKCNQ4
is asnp
is mentioned by
dbSNPrs797044966
dbSNP (old)rs797044966
ClinGenrs797044966
ebirs797044966
HLIrs797044966
Exacrs797044966
Varsomers797044966
Maprs797044966
PheGenIrs797044966
Biobankrs797044966
1000 genomesrs797044966
hgdprs797044966
ensemblrs797044966
gopubmedrs797044966
geneviewrs797044966
scholarrs797044966
googlers797044966
pharmgkbrs797044966
gwascentralrs797044966
openSNPrs797044966
23andMers797044966
23andMe allrs797044966
SNP Nexus

SNPshotrs797044966
SNPdbers797044966
MSV3drs797044966
GWAS Ctlgrs797044966
Max Magnitude0
ClinVar
Risk rs797044966(-;-)
Alt rs797044966(-;-)
Reference Rs797044966(CTC;CTC)
Significance Pathogenic
Disease DFNA 2 Nonsyndromic Hearing Loss not provided
Variation info
Gene KCNQ4
CLNDBN DFNA 2 Nonsyndromic Hearing Loss not provided
Reversed 0
HGVS NC_000001.10:g.41285116_41285118delCCT
CLNSRC
CLNACC RCV000194270.1, RCV000484405.1,