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rs786205226

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786205226(A;G)
Make rs786205226(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position11886025
GeneETV6
is asnp
is mentioned by
dbSNPrs786205226
ebirs786205226
HLIrs786205226
Exacrs786205226
Varsomers786205226
Maprs786205226
PheGenIrs786205226
hapmaprs786205226
1000 genomesrs786205226
hgdprs786205226
ensemblrs786205226
gopubmedrs786205226
geneviewrs786205226
scholarrs786205226
googlers786205226
pharmgkbrs786205226
gwascentralrs786205226
openSNPrs786205226
23andMers786205226
23andMe allrs786205226
SNP Nexus

SNPshotrs786205226
SNPdbers786205226
MSV3drs786205226
GWAS Ctlgrs786205226
Max Magnitude0
ClinVar
Risk rs786205226(G;G)
Alt rs786205226(G;G)
Reference rs786205226(A;A)
Significance Pathogenic
Disease Thrombocytopenia 5
Variation info
Gene ETV6
CLNDBN Thrombocytopenia 5
Reversed 0
HGVS NC_000012.11:g.12038959A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000170497.3,