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rs864321689

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AGAG;AGAG) 0 common in clinvar
Make rs864321689(-;-)
Make rs864321689(-;AGAG)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position28535746
GeneWAC
is asnp
is mentioned by
dbSNPrs864321689
dbSNP (old)rs864321689
ClinGenrs864321689
ebirs864321689
HLIrs864321689
Exacrs864321689
Gnomadrs864321689
Varsomers864321689
Maprs864321689
PheGenIrs864321689
Biobankrs864321689
1000 genomesrs864321689
hgdprs864321689
ensemblrs864321689
gopubmedrs864321689
geneviewrs864321689
scholarrs864321689
googlers864321689
pharmgkbrs864321689
gwascentralrs864321689
openSNPrs864321689
23andMers864321689
23andMe allrs864321689
SNP Nexus

SNPshotrs864321689
SNPdbers864321689
MSV3drs864321689
GWAS Ctlgrs864321689
Max Magnitude0
ClinVar
Risk rs864321689(-;-)
Alt rs864321689(-;-)
Reference Rs864321689(AGAG;AGAG)
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.28824675_28824678delAGAG
CLNSRC OMIM Allelic Variant
CLNACC RCV000203516.1, RCV000493235.1,