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rs1064796472

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome21
Position33552565
GeneSON
is asnp
is mentioned by
dbSNPrs1064796472
dbSNP (old)rs1064796472
ClinGenrs1064796472
ebirs1064796472
HLIrs1064796472
Exacrs1064796472
Gnomadrs1064796472
Varsomers1064796472
Maprs1064796472
PheGenIrs1064796472
Biobankrs1064796472
1000 genomesrs1064796472
hgdprs1064796472
ensemblrs1064796472
gopubmedrs1064796472
geneviewrs1064796472
scholarrs1064796472
googlers1064796472
pharmgkbrs1064796472
gwascentralrs1064796472
openSNPrs1064796472
23andMers1064796472
23andMe allrs1064796472
SNPshotrs1064796472
SNPdbers1064796472
MSV3drs1064796472
GWAS Ctlgrs1064796472
Max Magnitude0
ClinVar
Risk rs1064796472(T;T)
Alt rs1064796472(T;T)
Reference Rs1064796472(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene SON
CLNDBN not provided
Reversed 0
HGVS NC_000021.8:g.34924871C>T
CLNSRC
CLNACC RCV000482343.1,