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rs864321691

From SNPedia

Orientationplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs864321691(-;GG)
Make rs864321691(GG;GG)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position28535751
GeneWAC
is asnp
is mentioned by
dbSNPrs864321691
ClinGenrs864321691
ebirs864321691
HLIrs864321691
Exacrs864321691
Varsomers864321691
Maprs864321691
PheGenIrs864321691
hapmaprs864321691
1000 genomesrs864321691
hgdprs864321691
ensemblrs864321691
gopubmedrs864321691
geneviewrs864321691
scholarrs864321691
googlers864321691
pharmgkbrs864321691
gwascentralrs864321691
openSNPrs864321691
23andMers864321691
23andMe allrs864321691
SNP Nexus

SNPshotrs864321691
SNPdbers864321691
MSV3drs864321691
GWAS Ctlgrs864321691
Max Magnitude0
ClinVar
Risk rs864321691(GG;GG)
Alt rs864321691(GG;GG)
Reference Rs864321691(;)
Significance Pathogenic
Disease Desanto-shinawi syndrome
Variation info
Gene WAC
CLNDBN Desanto-shinawi syndrome
Reversed 0
HGVS NC_000010.10:g.28824679_28824680dupGG
CLNSRC OMIM Allelic Variant
CLNACC RCV000203559.1,