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rs864321634

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs864321634(C;T)
Make rs864321634(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position28617762
GeneWAC
is asnp
is mentioned by
dbSNPrs864321634
ebirs864321634
HLIrs864321634
Exacrs864321634
Varsomers864321634
Maprs864321634
PheGenIrs864321634
hapmaprs864321634
1000 genomesrs864321634
hgdprs864321634
ensemblrs864321634
gopubmedrs864321634
geneviewrs864321634
scholarrs864321634
googlers864321634
pharmgkbrs864321634
gwascentralrs864321634
openSNPrs864321634
23andMers864321634
23andMe allrs864321634
SNP Nexus

SNPshotrs864321634
SNPdbers864321634
MSV3drs864321634
GWAS Ctlgrs864321634
Max Magnitude0
ClinVar
Risk rs864321634(T;T)
Alt rs864321634(T;T)
Reference rs864321634(C;C)
Significance Pathogenic
Disease Desanto-shinawi syndrome
Variation info
Gene WAC
CLNDBN Desanto-shinawi syndrome
Reversed 0
HGVS NC_000010.10:g.28906691C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000203532.1,