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rs1057521155

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057521155(C;C)
Make rs1057521155(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position189575169
GeneSLC40A1
is asnp
is mentioned by
dbSNPrs1057521155
dbSNP (old)rs1057521155
ClinGenrs1057521155
ebirs1057521155
HLIrs1057521155
Exacrs1057521155
Gnomadrs1057521155
Varsomers1057521155
Maprs1057521155
PheGenIrs1057521155
Biobankrs1057521155
1000 genomesrs1057521155
hgdprs1057521155
ensemblrs1057521155
gopubmedrs1057521155
geneviewrs1057521155
scholarrs1057521155
googlers1057521155
pharmgkbrs1057521155
gwascentralrs1057521155
openSNPrs1057521155
23andMers1057521155
23andMe allrs1057521155
SNPshotrs1057521155
SNPdbers1057521155
MSV3drs1057521155
GWAS Ctlgrs1057521155
Max Magnitude0
ClinVar
Risk rs1057521155(C;C)
Alt rs1057521155(C;C)
Reference Rs1057521155(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SLC40A1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.190439895C>G
CLNSRC
CLNACC RCV000435183.1,