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rs587778515

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587778515(-;-)
Make rs587778515(-;T)
ReferenceGRCh38.p7 38.3/149
Chromosome1
Position43338705
GeneMPL
is asnp
is mentioned by
dbSNPrs587778515
dbSNP (classic)rs587778515
ClinGenrs587778515
ebirs587778515
HLIrs587778515
Exacrs587778515
Gnomadrs587778515
Varsomers587778515
LitVarrs587778515
Maprs587778515
PheGenIrs587778515
Biobankrs587778515
1000 genomesrs587778515
hgdprs587778515
ensemblrs587778515
geneviewrs587778515
scholarrs587778515
googlers587778515
pharmgkbrs587778515
gwascentralrs587778515
openSNPrs587778515
23andMers587778515
SNPshotrs587778515
SNPdbers587778515
MSV3drs587778515
GWAS Ctlgrs587778515
Merged fromRs886039426
Max Magnitude0
ClinVar
Risk rs587778515(-;-)
Alt rs587778515(-;-)
Reference Rs587778515(T;T)
Significance Pathogenic
Disease not specified not provided
Variation info
Gene MPL
CLNDBN not specified not provided
Reversed 0
HGVS NC_000001.10:g.43804378delT
CLNSRC
CLNACC RCV000121537.1, RCV000255711.1,