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rs886039426

From SNPedia

Merged intors587778515
Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs886039426(-;-)
Make rs886039426(-;T)
ReferenceGRCh38.p7 38.3/149
Chromosome1
Position43338707
GeneMPL
is asnp
is mentioned by
dbSNPrs886039426
dbSNP (classic)rs886039426
ClinGenrs886039426
ebirs886039426
HLIrs886039426
Exacrs886039426
Gnomadrs886039426
Varsomers886039426
LitVarrs886039426
Maprs886039426
PheGenIrs886039426
Biobankrs886039426
1000 genomesrs886039426
hgdprs886039426
ensemblrs886039426
geneviewrs886039426
scholarrs886039426
googlers886039426
pharmgkbrs886039426
gwascentralrs886039426
openSNPrs886039426
23andMers886039426
SNPshotrs886039426
SNPdbers886039426
MSV3drs886039426
GWAS Ctlgrs886039426
StatusMerged into rs587778515
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs886039426(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,