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rs886039676

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs886039676(C;G)
Make rs886039676(G;G)
ReferenceGRCh38.p7 38.3/149
Chromosome6
Position157181096
GeneARID1B
is asnp
is mentioned by
dbSNPrs886039676
dbSNP (classic)rs886039676
ClinGenrs886039676
ebirs886039676
HLIrs886039676
Exacrs886039676
Gnomadrs886039676
Varsomers886039676
LitVarrs886039676
Maprs886039676
PheGenIrs886039676
Biobankrs886039676
1000 genomesrs886039676
hgdprs886039676
ensemblrs886039676
geneviewrs886039676
scholarrs886039676
googlers886039676
pharmgkbrs886039676
gwascentralrs886039676
openSNPrs886039676
23andMers886039676
SNPshotrs886039676
SNPdbers886039676
MSV3drs886039676
GWAS Ctlgrs886039676
Max Magnitude0
ClinVar
Risk rs886039676(G;G)
Alt rs886039676(G;G)
Reference Rs886039676(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene ARID1B
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.157502230C>G
CLNSRC
CLNACC RCV000255840.1,