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rs1057517839

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057517839(A;G)
Make rs1057517839(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position46701579
GeneTMIE
is asnp
is mentioned by
dbSNPrs1057517839
dbSNP (old)rs1057517839
ClinGenrs1057517839
ebirs1057517839
HLIrs1057517839
Exacrs1057517839
Gnomadrs1057517839
Varsomers1057517839
Maprs1057517839
PheGenIrs1057517839
Biobankrs1057517839
1000 genomesrs1057517839
hgdprs1057517839
ensemblrs1057517839
gopubmedrs1057517839
geneviewrs1057517839
scholarrs1057517839
googlers1057517839
pharmgkbrs1057517839
gwascentralrs1057517839
openSNPrs1057517839
23andMers1057517839
23andMe allrs1057517839
SNPshotrs1057517839
SNPdbers1057517839
MSV3drs1057517839
GWAS Ctlgrs1057517839
Max Magnitude0
ClinVar
Risk rs1057517839(G;G)
Alt rs1057517839(G;G)
Reference Rs1057517839(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene TMIE
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.46743069A>G
CLNSRC
CLNACC RCV000414718.1,