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rs886039699

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs886039699(A;A)
Make rs886039699(A;G)
ReferenceGRCh38.p7 38.3/149
Chromosome6
Position157184436
GeneARID1B
is asnp
is mentioned by
dbSNPrs886039699
dbSNP (classic)rs886039699
ClinGenrs886039699
ebirs886039699
HLIrs886039699
Exacrs886039699
Gnomadrs886039699
Varsomers886039699
LitVarrs886039699
Maprs886039699
PheGenIrs886039699
Biobankrs886039699
1000 genomesrs886039699
hgdprs886039699
ensemblrs886039699
geneviewrs886039699
scholarrs886039699
googlers886039699
pharmgkbrs886039699
gwascentralrs886039699
openSNPrs886039699
23andMers886039699
SNPshotrs886039699
SNPdbers886039699
MSV3drs886039699
GWAS Ctlgrs886039699
Max Magnitude0
ClinVar
Risk rs886039699(A;A)
Alt rs886039699(A;A)
Reference Rs886039699(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ARID1B
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.157505570G>A
CLNSRC
CLNACC RCV000256015.1,