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rs876657382

From SNPedia

Orientationplus
Geno Mag Summary
(ACCAGACGCC;ACCAGACGCC) 0 common in clinvar
Make rs876657382(-;-)
Make rs876657382(-;ACCAGACGCC)
ReferenceGRCh38.p2 38.2/147
Chromosome6
Position157201213
GeneARID1B
is asnp
is mentioned by
dbSNPrs876657382
ebirs876657382
HLIrs876657382
Exacrs876657382
Varsomers876657382
Maprs876657382
PheGenIrs876657382
hapmaprs876657382
1000 genomesrs876657382
hgdprs876657382
ensemblrs876657382
gopubmedrs876657382
geneviewrs876657382
scholarrs876657382
googlers876657382
pharmgkbrs876657382
gwascentralrs876657382
openSNPrs876657382
23andMers876657382
23andMe allrs876657382
SNP Nexus

SNPshotrs876657382
SNPdbers876657382
MSV3drs876657382
GWAS Ctlgrs876657382
Max Magnitude0
ClinVar
Risk rs876657382(;)
Alt rs876657382(;)
Reference rs876657382(ACCAGACGCC;ACCAGACGCC)
Significance Pathogenic
Disease Coffin-Siris syndrome
Variation info
Gene ARID1B
CLNDBN Coffin-Siris syndrome
Reversed 0
HGVS NC_000006.11:g.157522347_157522356delACCAGACGCC
CLNSRC OMIM Allelic Variant
CLNACC RCV000024216.4,