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rs387907141

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387907141(C;T)
Make rs387907141(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position157181137
GeneARID1B
is asnp
is mentioned by
dbSNPrs387907141
ebirs387907141
HLIrs387907141
Exacrs387907141
Varsomers387907141
Maprs387907141
PheGenIrs387907141
hapmaprs387907141
1000 genomesrs387907141
hgdprs387907141
ensemblrs387907141
gopubmedrs387907141
geneviewrs387907141
scholarrs387907141
googlers387907141
pharmgkbrs387907141
gwascentralrs387907141
openSNPrs387907141
23andMers387907141
23andMe allrs387907141
SNP Nexus

SNPshotrs387907141
SNPdbers387907141
MSV3drs387907141
GWAS Ctlgrs387907141
Max Magnitude0
ClinVar
Risk rs387907141(T;T)
Alt rs387907141(T;T)
Reference rs387907141(C;C)
Significance Pathogenic
Disease Coffin-Siris syndrome
Variation info
Gene ARID1B
CLNDBN Coffin-Siris syndrome
Reversed 0
HGVS NC_000006.11:g.157502271C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000024209.3,