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rs1064795433

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome11
Position119029224
GeneSLC37A4
is asnp
is mentioned by
dbSNPrs1064795433
dbSNP (old)rs1064795433
ClinGenrs1064795433
ebirs1064795433
HLIrs1064795433
Exacrs1064795433
Gnomadrs1064795433
Varsomers1064795433
Maprs1064795433
PheGenIrs1064795433
Biobankrs1064795433
1000 genomesrs1064795433
hgdprs1064795433
ensemblrs1064795433
gopubmedrs1064795433
geneviewrs1064795433
scholarrs1064795433
googlers1064795433
pharmgkbrs1064795433
gwascentralrs1064795433
openSNPrs1064795433
23andMers1064795433
23andMe allrs1064795433
SNPshotrs1064795433
SNPdbers1064795433
MSV3drs1064795433
GWAS Ctlgrs1064795433
Max Magnitude0
ClinVar
Risk rs1064795433(-;-)
Alt rs1064795433(-;-)
Reference Rs1064795433(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SLC37A4
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.118899934delA
CLNSRC
CLNACC RCV000485927.1,