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rs876657380

From SNPedia

Orientationplus
Geno Mag Summary
(AA;AA) 0 common in clinvar
Make rs876657380(-;-)
Make rs876657380(-;AA)
ReferenceGRCh38.p2 38.2/147
Chromosome6
Position157181156
GeneARID1B
is asnp
is mentioned by
dbSNPrs876657380
ebirs876657380
HLIrs876657380
Exacrs876657380
Varsomers876657380
Maprs876657380
PheGenIrs876657380
hapmaprs876657380
1000 genomesrs876657380
hgdprs876657380
ensemblrs876657380
gopubmedrs876657380
geneviewrs876657380
scholarrs876657380
googlers876657380
pharmgkbrs876657380
gwascentralrs876657380
openSNPrs876657380
23andMers876657380
23andMe allrs876657380
SNP Nexus

SNPshotrs876657380
SNPdbers876657380
MSV3drs876657380
GWAS Ctlgrs876657380
Max Magnitude0
ClinVar
Risk rs876657380(;)
Alt rs876657380(;)
Reference rs876657380(AA;AA)
Significance Pathogenic
Disease Coffin-Siris syndrome
Variation info
Gene ARID1B
CLNDBN Coffin-Siris syndrome
Reversed 0
HGVS NC_000006.11:g.157502290_157502291delAA
CLNSRC OMIM Allelic Variant
CLNACC RCV000024210.4,