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rs104893964

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104893964(A;A)
Make rs104893964(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position121446912
GeneGJA1
is asnp
is mentioned by
dbSNPrs104893964
ebirs104893964
HLIrs104893964
Exacrs104893964
Varsomers104893964
Maprs104893964
PheGenIrs104893964
hapmaprs104893964
1000 genomesrs104893964
hgdprs104893964
ensemblrs104893964
gopubmedrs104893964
geneviewrs104893964
scholarrs104893964
googlers104893964
pharmgkbrs104893964
gwascentralrs104893964
openSNPrs104893964
23andMers104893964
23andMe allrs104893964
SNP Nexus

SNPshotrs104893964
SNPdbers104893964
MSV3drs104893964
GWAS Ctlgrs104893964
Max Magnitude0
OMIM121014
Desc
Variant0006
Relatedalso
ClinVar
Risk rs104893964(A;A)
Alt rs104893964(A;A)
Reference rs104893964(G;G)
Significance Pathogenic
Disease Oculodentodigital dysplasia
Variation info
Gene GJA1
CLNDBN Oculodentodigital dysplasia
Reversed 0
HGVS NC_000006.11:g.121768058G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000018506.28,