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rs727504635

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs727504635(-;-)
Make rs727504635(-;C)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position40818217
GeneKCNQ4
is asnp
is mentioned by
dbSNPrs727504635
ebirs727504635
HLIrs727504635
Exacrs727504635
Varsomers727504635
Maprs727504635
PheGenIrs727504635
hapmaprs727504635
1000 genomesrs727504635
hgdprs727504635
ensemblrs727504635
gopubmedrs727504635
geneviewrs727504635
scholarrs727504635
googlers727504635
pharmgkbrs727504635
gwascentralrs727504635
openSNPrs727504635
23andMers727504635
23andMe allrs727504635
SNP Nexus

SNPshotrs727504635
SNPdbers727504635
MSV3drs727504635
GWAS Ctlgrs727504635
Max Magnitude0
ClinVar
Risk rs727504635(;)
Alt rs727504635(;)
Reference rs727504635(C;C)
Significance Pathogenic
Disease Non-syndromic genetic deafness
Variation info
Gene KCNQ4
CLNDBN Non-syndromic genetic deafness
Reversed 0
HGVS NC_000001.10:g.41283889delC
CLNSRC
CLNACC RCV000155896.1,