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rs864321693

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs864321693(-;-)
Make rs864321693(-;A)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position28535595
GeneWAC
is asnp
is mentioned by
dbSNPrs864321693
dbSNP (classic)rs864321693
ClinGenrs864321693
ebirs864321693
HLIrs864321693
Exacrs864321693
Gnomadrs864321693
Varsomers864321693
LitVarrs864321693
Maprs864321693
PheGenIrs864321693
Biobankrs864321693
1000 genomesrs864321693
hgdprs864321693
ensemblrs864321693
geneviewrs864321693
scholarrs864321693
googlers864321693
pharmgkbrs864321693
gwascentralrs864321693
openSNPrs864321693
23andMers864321693
SNPshotrs864321693
SNPdbers864321693
MSV3drs864321693
GWAS Ctlgrs864321693
Max Magnitude0
ClinVar
Risk rs864321693(-;-)
Alt rs864321693(-;-)
Reference Rs864321693(A;A)
Significance Pathogenic
Disease Desanto-shinawi syndrome not provided
Variation info
Gene WAC
CLNDBN Desanto-shinawi syndrome not provided
Reversed 0
HGVS NC_000010.10:g.28824524delA
CLNSRC OMIM Allelic Variant
CLNACC RCV000203557.1, RCV000485468.1,