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rs864321692

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs864321692(A;A)
Make rs864321692(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position28583498
GeneWAC
is asnp
is mentioned by
dbSNPrs864321692
ebirs864321692
HLIrs864321692
Exacrs864321692
Varsomers864321692
Maprs864321692
PheGenIrs864321692
hapmaprs864321692
1000 genomesrs864321692
hgdprs864321692
ensemblrs864321692
gopubmedrs864321692
geneviewrs864321692
scholarrs864321692
googlers864321692
pharmgkbrs864321692
gwascentralrs864321692
openSNPrs864321692
23andMers864321692
23andMe allrs864321692
SNP Nexus

SNPshotrs864321692
SNPdbers864321692
MSV3drs864321692
GWAS Ctlgrs864321692
Max Magnitude0
ClinVar
Risk rs864321692(A;A)
Alt rs864321692(A;A)
Reference rs864321692(C;C)
Significance Pathogenic
Disease Desanto-shinawi syndrome
Variation info
Gene WAC
CLNDBN Desanto-shinawi syndrome
Reversed 0
HGVS NC_000010.10:g.28872427C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000203521.1,