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rs876657381

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876657381(-;-)
Make rs876657381(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome6
Position157206773
GeneARID1B
is asnp
is mentioned by
dbSNPrs876657381
ebirs876657381
HLIrs876657381
Exacrs876657381
Varsomers876657381
Maprs876657381
PheGenIrs876657381
hapmaprs876657381
1000 genomesrs876657381
hgdprs876657381
ensemblrs876657381
gopubmedrs876657381
geneviewrs876657381
scholarrs876657381
googlers876657381
pharmgkbrs876657381
gwascentralrs876657381
openSNPrs876657381
23andMers876657381
23andMe allrs876657381
SNP Nexus

SNPshotrs876657381
SNPdbers876657381
MSV3drs876657381
GWAS Ctlgrs876657381
Max Magnitude0
ClinVar
Risk rs876657381(;)
Alt rs876657381(;)
Reference rs876657381(G;G)
Significance Pathogenic
Disease Coffin-Siris syndrome
Variation info
Gene ARID1B
CLNDBN Coffin-Siris syndrome
Reversed 0
HGVS NC_000006.11:g.157527907delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000024213.4,