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rs869312956

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869312956(A;A)
Make rs869312956(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position26780130
GeneARID1A
is asnp
is mentioned by
dbSNPrs869312956
ebirs869312956
HLIrs869312956
Exacrs869312956
Varsomers869312956
Maprs869312956
PheGenIrs869312956
hapmaprs869312956
1000 genomesrs869312956
hgdprs869312956
ensemblrs869312956
gopubmedrs869312956
geneviewrs869312956
scholarrs869312956
googlers869312956
pharmgkbrs869312956
gwascentralrs869312956
openSNPrs869312956
23andMers869312956
23andMe allrs869312956
SNP Nexus

SNPshotrs869312956
SNPdbers869312956
MSV3drs869312956
GWAS Ctlgrs869312956
Max Magnitude0
ClinVar
Risk rs869312956(A;A)
Alt rs869312956(A;A)
Reference rs869312956(G;G)
Significance Probable-Pathogenic
Disease Inborn genetic diseases
Variation info
Gene ARID1A
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000001.10:g.27106621G>A
CLNSRC
CLNACC RCV000210642.1,