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rs1057518984

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518984(A;A)
Make rs1057518984(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position157203997
GeneARID1B
is asnp
is mentioned by
dbSNPrs1057518984
dbSNP (old)rs1057518984
ClinGenrs1057518984
ebirs1057518984
HLIrs1057518984
Exacrs1057518984
Gnomadrs1057518984
Varsomers1057518984
LitVarrs1057518984
Maprs1057518984
PheGenIrs1057518984
Biobankrs1057518984
1000 genomesrs1057518984
hgdprs1057518984
ensemblrs1057518984
gopubmedrs1057518984
geneviewrs1057518984
scholarrs1057518984
googlers1057518984
pharmgkbrs1057518984
gwascentralrs1057518984
openSNPrs1057518984
23andMers1057518984
23andMe allrs1057518984
SNPshotrs1057518984
SNPdbers1057518984
MSV3drs1057518984
GWAS Ctlgrs1057518984
Max Magnitude0
ClinVar
Risk rs1057518984(A;A)
Alt rs1057518984(A;A)
Reference Rs1057518984(G;G)
Significance Probable-Pathogenic
Disease Coffin-Siris syndrome
Variation info
Gene ARID1B
CLNDBN Coffin-Siris syndrome
Reversed 0
HGVS NC_000006.11:g.157525131G>A
CLNSRC
CLNACC RCV000414844.1,