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rs267606856

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267606856(C;T)
Make rs267606856(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position42962919
GeneGRXCR1
is asnp
is mentioned by
dbSNPrs267606856
ebirs267606856
HLIrs267606856
Exacrs267606856
Varsomers267606856
Maprs267606856
PheGenIrs267606856
hapmaprs267606856
1000 genomesrs267606856
hgdprs267606856
ensemblrs267606856
gopubmedrs267606856
geneviewrs267606856
scholarrs267606856
googlers267606856
pharmgkbrs267606856
gwascentralrs267606856
openSNPrs267606856
23andMers267606856
23andMe allrs267606856
SNP Nexus

SNPshotrs267606856
SNPdbers267606856
MSV3drs267606856
GWAS Ctlgrs267606856
Max Magnitude0
ClinVar
Risk rs267606856(T;T)
Alt rs267606856(T;T)
Reference rs267606856(C;C)
Significance Pathogenic
Disease Deafness
Variation info
Gene GRXCR1
CLNDBN Deafness, autosomal recessive 25
Reversed 0
HGVS NC_000004.11:g.42964936C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000000219.2,