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rs886039679

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs886039679(A;A)
Make rs886039679(A;G)
ReferenceGRCh38.p7 38.3/149
Chromosome6
Position157167186
GeneARID1B
is asnp
is mentioned by
dbSNPrs886039679
dbSNP (classic)rs886039679
ClinGenrs886039679
ebirs886039679
HLIrs886039679
Exacrs886039679
Gnomadrs886039679
Varsomers886039679
LitVarrs886039679
Maprs886039679
PheGenIrs886039679
Biobankrs886039679
1000 genomesrs886039679
hgdprs886039679
ensemblrs886039679
geneviewrs886039679
scholarrs886039679
googlers886039679
pharmgkbrs886039679
gwascentralrs886039679
openSNPrs886039679
23andMers886039679
SNPshotrs886039679
SNPdbers886039679
MSV3drs886039679
GWAS Ctlgrs886039679
Max Magnitude0
ClinVar
Risk rs886039679(A;A)
Alt rs886039679(A;A)
Reference Rs886039679(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ARID1B
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.157488320G>A
CLNSRC
CLNACC RCV000255997.1,