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rs1064795684

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome8
Position42437204
GeneSLC20A2
is asnp
is mentioned by
dbSNPrs1064795684
dbSNP (classic)rs1064795684
ClinGenrs1064795684
ebirs1064795684
HLIrs1064795684
Exacrs1064795684
Gnomadrs1064795684
Varsomers1064795684
LitVarrs1064795684
Maprs1064795684
PheGenIrs1064795684
Biobankrs1064795684
1000 genomesrs1064795684
hgdprs1064795684
ensemblrs1064795684
geneviewrs1064795684
scholarrs1064795684
googlers1064795684
pharmgkbrs1064795684
gwascentralrs1064795684
openSNPrs1064795684
23andMers1064795684
23andMe allrs1064795684
SNPshotrs1064795684
SNPdbers1064795684
MSV3drs1064795684
GWAS Ctlgrs1064795684
Max Magnitude0
ClinVar
Risk rs1064795684(G;G)
Alt rs1064795684(G;G)
Reference Rs1064795684(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SLC20A2
CLNDBN not provided
Reversed 1
HGVS NC_000008.10:g.42294722G>C
CLNSRC
CLNACC RCV000485134.1,