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rs267606845

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267606845(A;A)
Make rs267606845(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position121447073
GeneGJA1
is asnp
is mentioned by
dbSNPrs267606845
dbSNP (classic)rs267606845
ClinGenrs267606845
ebirs267606845
HLIrs267606845
Exacrs267606845
Gnomadrs267606845
Varsomers267606845
LitVarrs267606845
Maprs267606845
PheGenIrs267606845
Biobankrs267606845
1000 genomesrs267606845
hgdprs267606845
ensemblrs267606845
geneviewrs267606845
scholarrs267606845
googlers267606845
pharmgkbrs267606845
gwascentralrs267606845
openSNPrs267606845
23andMers267606845
SNPshotrs267606845
SNPdbers267606845
MSV3drs267606845
GWAS Ctlgrs267606845
Max Magnitude0
ClinVar
Risk rs267606845(A;A)
Alt rs267606845(A;A)
Reference Rs267606845(C;C)
Significance Other
Disease Oculodentodigital dysplasia not provided
Variation info
Gene GJA1
CLNDBN Oculodentodigital dysplasia not provided
Reversed 0
HGVS NC_000006.11:g.121768219C>A
CLNSRC OMIM Allelic Variant UniProtKB (protein)
CLNACC RCV000018520.31, RCV000430201.1,