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rs1057521727

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057521727(A;A)
Make rs1057521727(A;C)
ReferenceGRCh38.p7 38.3/150
Chromosome4
Position102267942
GeneSLC39A8
is asnp
is mentioned by
dbSNPrs1057521727
dbSNP (old)rs1057521727
ClinGenrs1057521727
ebirs1057521727
HLIrs1057521727
Exacrs1057521727
Gnomadrs1057521727
Varsomers1057521727
Maprs1057521727
PheGenIrs1057521727
Biobankrs1057521727
1000 genomesrs1057521727
hgdprs1057521727
ensemblrs1057521727
gopubmedrs1057521727
geneviewrs1057521727
scholarrs1057521727
googlers1057521727
pharmgkbrs1057521727
gwascentralrs1057521727
openSNPrs1057521727
23andMers1057521727
23andMe allrs1057521727
SNPshotrs1057521727
SNPdbers1057521727
MSV3drs1057521727
GWAS Ctlgrs1057521727
Max Magnitude0
ClinVar
Risk rs1057521727(A;A)
Alt rs1057521727(A;A)
Reference Rs1057521727(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SLC39A8
CLNDBN not provided
Reversed 1
HGVS NC_000004.11:g.103189099G>T
CLNSRC
CLNACC RCV000439449.1,