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rs267606855

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267606855(C;T)
Make rs267606855(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position42893495
GeneGRXCR1
is asnp
is mentioned by
dbSNPrs267606855
ebirs267606855
HLIrs267606855
Exacrs267606855
Varsomers267606855
Maprs267606855
PheGenIrs267606855
hapmaprs267606855
1000 genomesrs267606855
hgdprs267606855
ensemblrs267606855
gopubmedrs267606855
geneviewrs267606855
scholarrs267606855
googlers267606855
pharmgkbrs267606855
gwascentralrs267606855
openSNPrs267606855
23andMers267606855
23andMe allrs267606855
SNP Nexus

SNPshotrs267606855
SNPdbers267606855
MSV3drs267606855
GWAS Ctlgrs267606855
Max Magnitude0
ClinVar
Risk rs267606855(T;T)
Alt rs267606855(T;T)
Reference rs267606855(C;C)
Significance Pathogenic
Disease Deafness
Variation info
Gene GRXCR1
CLNDBN Deafness, autosomal recessive 25
Reversed 0
HGVS NC_000004.11:g.42895512C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000000218.2,