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rs1057517761

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057517761(C;C)
Make rs1057517761(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position43349004
GeneMPL
is asnp
is mentioned by
dbSNPrs1057517761
dbSNP (old)rs1057517761
ClinGenrs1057517761
ebirs1057517761
HLIrs1057517761
Exacrs1057517761
Gnomadrs1057517761
Varsomers1057517761
LitVarrs1057517761
Maprs1057517761
PheGenIrs1057517761
Biobankrs1057517761
1000 genomesrs1057517761
hgdprs1057517761
ensemblrs1057517761
gopubmedrs1057517761
geneviewrs1057517761
scholarrs1057517761
googlers1057517761
pharmgkbrs1057517761
gwascentralrs1057517761
openSNPrs1057517761
23andMers1057517761
23andMe allrs1057517761
SNPshotrs1057517761
SNPdbers1057517761
MSV3drs1057517761
GWAS Ctlgrs1057517761
Max Magnitude0
ClinVar
Risk rs1057517761(C;C)
Alt rs1057517761(C;C)
Reference Rs1057517761(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene MPL
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.43814675T>C
CLNSRC
CLNACC RCV000412964.1,