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rs1064793985

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(AT;AT) 0 common in clinvar
Chromosome21
Position46416284
GenePCNT
is asnp
is mentioned by
dbSNPrs1064793985
dbSNP (old)rs1064793985
ClinGenrs1064793985
ebirs1064793985
HLIrs1064793985
Exacrs1064793985
Gnomadrs1064793985
Varsomers1064793985
Maprs1064793985
PheGenIrs1064793985
Biobankrs1064793985
1000 genomesrs1064793985
hgdprs1064793985
ensemblrs1064793985
gopubmedrs1064793985
geneviewrs1064793985
scholarrs1064793985
googlers1064793985
pharmgkbrs1064793985
gwascentralrs1064793985
openSNPrs1064793985
23andMers1064793985
23andMe allrs1064793985
SNPshotrs1064793985
SNPdbers1064793985
MSV3drs1064793985
GWAS Ctlgrs1064793985
Max Magnitude0
ClinVar
Risk rs1064793985(-;-)
Alt rs1064793985(-;-)
Reference Rs1064793985(AT;AT)
Significance Pathogenic
Disease not provided
Variation info
Gene PCNT
CLNDBN not provided
Reversed 0
HGVS NC_000021.8:g.47836198_47836199delAT
CLNSRC
CLNACC RCV000480431.1,