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rs750447037

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs750447037(A;A)
Make rs750447037(A;C)
ReferenceGRCh38.p7 38.3/149
Chromosome6
Position157206479
GeneARID1B
is asnp
is mentioned by
dbSNPrs750447037
dbSNP (classic)rs750447037
ClinGenrs750447037
ebirs750447037
HLIrs750447037
Exacrs750447037
Gnomadrs750447037
Varsomers750447037
LitVarrs750447037
Maprs750447037
PheGenIrs750447037
Biobankrs750447037
1000 genomesrs750447037
hgdprs750447037
ensemblrs750447037
geneviewrs750447037
scholarrs750447037
googlers750447037
pharmgkbrs750447037
gwascentralrs750447037
openSNPrs750447037
23andMers750447037
SNPshotrs750447037
SNPdbers750447037
MSV3drs750447037
GWAS Ctlgrs750447037
Max Magnitude0
ClinVar
Risk rs750447037(A;A) rs750447037(T;T)
Alt rs750447037(A;A) rs750447037(T;T)
Reference Rs750447037(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene ARID1B
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.157527613C>T
CLNSRC
CLNACC RCV000276336.1,