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rs724159945

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs724159945(C;T)
Make rs724159945(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome12
Position11885968
GeneETV6
is asnp
is mentioned by
dbSNPrs724159945
ebirs724159945
HLIrs724159945
Exacrs724159945
Varsomers724159945
Maprs724159945
PheGenIrs724159945
hapmaprs724159945
1000 genomesrs724159945
hgdprs724159945
ensemblrs724159945
gopubmedrs724159945
geneviewrs724159945
scholarrs724159945
googlers724159945
pharmgkbrs724159945
gwascentralrs724159945
openSNPrs724159945
23andMers724159945
23andMe allrs724159945
SNP Nexus

SNPshotrs724159945
SNPdbers724159945
MSV3drs724159945
GWAS Ctlgrs724159945
Max Magnitude0
ClinVar
Risk rs724159945(T;T)
Alt rs724159945(T;T)
Reference rs724159945(C;C)
Significance Pathogenic
Disease Hematologic neoplasm Thrombocytopenia Thrombocytopenia 5
Variation info
Gene ETV6
CLNDBN Hematologic neoplasm Thrombocytopenia Thrombocytopenia 5
Reversed 0
HGVS NC_000012.11:g.12038902C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000149802.1, RCV000157609.3,