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rs1064793729

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
ChromosomeX
Position21606880
GeneCNKSR2
is asnp
is mentioned by
dbSNPrs1064793729
dbSNP (old)rs1064793729
ClinGenrs1064793729
ebirs1064793729
HLIrs1064793729
Exacrs1064793729
Gnomadrs1064793729
Varsomers1064793729
LitVarrs1064793729
Maprs1064793729
PheGenIrs1064793729
Biobankrs1064793729
1000 genomesrs1064793729
hgdprs1064793729
ensemblrs1064793729
gopubmedrs1064793729
geneviewrs1064793729
scholarrs1064793729
googlers1064793729
pharmgkbrs1064793729
gwascentralrs1064793729
openSNPrs1064793729
23andMers1064793729
23andMe allrs1064793729
SNPshotrs1064793729
SNPdbers1064793729
MSV3drs1064793729
GWAS Ctlgrs1064793729
Max Magnitude0
ClinVar
Risk rs1064793729(A;A)
Alt rs1064793729(A;A)
Reference Rs1064793729(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene CNKSR2
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.21624998G>A
CLNSRC
CLNACC RCV000482744.1,