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rs1064793462

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(CA;CA) 0 common in clinvar
Chromosome19
Position36104628
GeneWDR62
is asnp
is mentioned by
dbSNPrs1064793462
dbSNP (old)rs1064793462
ClinGenrs1064793462
ebirs1064793462
HLIrs1064793462
Exacrs1064793462
Gnomadrs1064793462
Varsomers1064793462
Maprs1064793462
PheGenIrs1064793462
Biobankrs1064793462
1000 genomesrs1064793462
hgdprs1064793462
ensemblrs1064793462
gopubmedrs1064793462
geneviewrs1064793462
scholarrs1064793462
googlers1064793462
pharmgkbrs1064793462
gwascentralrs1064793462
openSNPrs1064793462
23andMers1064793462
23andMe allrs1064793462
SNPshotrs1064793462
SNPdbers1064793462
MSV3drs1064793462
GWAS Ctlgrs1064793462
Max Magnitude0
ClinVar
Risk rs1064793462(GTGGTCTGAG;GTGGTCTGAG)
Alt rs1064793462(GTGGTCTGAG;GTGGTCTGAG)
Reference Rs1064793462(CA;CA)
Significance Pathogenic
Disease not provided
Variation info
Gene WDR62
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.36595530_36595531delCAinsGTGGTCTGAG
CLNSRC
CLNACC RCV000480506.1,