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rs864321690

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs864321690(A;A)
Make rs864321690(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position28616337
GeneWAC
is asnp
is mentioned by
dbSNPrs864321690
ebirs864321690
HLIrs864321690
Exacrs864321690
Varsomers864321690
Maprs864321690
PheGenIrs864321690
hapmaprs864321690
1000 genomesrs864321690
hgdprs864321690
ensemblrs864321690
gopubmedrs864321690
geneviewrs864321690
scholarrs864321690
googlers864321690
pharmgkbrs864321690
gwascentralrs864321690
openSNPrs864321690
23andMers864321690
23andMe allrs864321690
SNP Nexus

SNPshotrs864321690
SNPdbers864321690
MSV3drs864321690
GWAS Ctlgrs864321690
Max Magnitude0
ClinVar
Risk rs864321690(A;A)
Alt rs864321690(A;A)
Reference rs864321690(G;G)
Significance Pathogenic
Disease Desanto-shinawi syndrome
Variation info
Gene WAC
CLNDBN Desanto-shinawi syndrome
Reversed 0
HGVS NC_000010.10:g.28905266G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000203534.1,