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rs1064796985

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome4
Position39205588
GeneWDR19
is asnp
is mentioned by
dbSNPrs1064796985
dbSNP (old)rs1064796985
ClinGenrs1064796985
ebirs1064796985
HLIrs1064796985
Exacrs1064796985
Gnomadrs1064796985
Varsomers1064796985
Maprs1064796985
PheGenIrs1064796985
Biobankrs1064796985
1000 genomesrs1064796985
hgdprs1064796985
ensemblrs1064796985
gopubmedrs1064796985
geneviewrs1064796985
scholarrs1064796985
googlers1064796985
pharmgkbrs1064796985
gwascentralrs1064796985
openSNPrs1064796985
23andMers1064796985
23andMe allrs1064796985
SNPshotrs1064796985
SNPdbers1064796985
MSV3drs1064796985
GWAS Ctlgrs1064796985
Max Magnitude0
ClinVar
Risk rs1064796985(A;A)
Alt rs1064796985(A;A)
Reference Rs1064796985(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene WDR19
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.39207208G>A
CLNSRC
CLNACC RCV000484356.1,