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rs146249964

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;T) 3 Carrier of a congenital amegakaryocytic thrombocytopenia mutation
(T;T) 0 common in clinvar


Make rs146249964(A;A)
ReferenceGRCh38.p7 38.3/149
Chromosome1
Position43337929
GeneMPL
is asnp
is mentioned by
dbSNPrs146249964
dbSNP (classic)rs146249964
ClinGenrs146249964
ebirs146249964
HLIrs146249964
Exacrs146249964
Gnomadrs146249964
Varsomers146249964
LitVarrs146249964
Maprs146249964
PheGenIrs146249964
Biobankrs146249964
1000 genomesrs146249964
hgdprs146249964
ensemblrs146249964
geneviewrs146249964
scholarrs146249964
googlers146249964
pharmgkbrs146249964
gwascentralrs146249964
openSNPrs146249964
23andMers146249964
SNPshotrs146249964
SNPdbers146249964
MSV3drs146249964
GWAS Ctlgrs146249964
Max Magnitude3

aka c.79+2T>A

This variant in the thrombopoietin receptor-encoding gene, MPL, was reported in 2011 to be a founder mutation the Ashkenazi Jewish (AJ) population for CAMT (congenital amegakaryocytic thrombocytopenia), and the carrier frequency was estimated to be 1 in 75.[PMID 21489838]

ClinVar
Risk rs146249964(A;A)
Alt rs146249964(A;A)
Reference Rs146249964(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.43803600T>A
CLNSRC
CLNACC RCV000122423.1, RCV000254762.1,