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rs786205154

From SNPedia

Orientationplus
Geno Mag Summary
(AACAG;AACAG) 0 common in clinvar
Make rs786205154(-;-)
Make rs786205154(-;AACAG)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position11885921
GeneETV6
is asnp
is mentioned by
dbSNPrs786205154
ebirs786205154
HLIrs786205154
Exacrs786205154
Varsomers786205154
Maprs786205154
PheGenIrs786205154
hapmaprs786205154
1000 genomesrs786205154
hgdprs786205154
ensemblrs786205154
gopubmedrs786205154
geneviewrs786205154
scholarrs786205154
googlers786205154
pharmgkbrs786205154
gwascentralrs786205154
openSNPrs786205154
23andMers786205154
23andMe allrs786205154
SNP Nexus

SNPshotrs786205154
SNPdbers786205154
MSV3drs786205154
GWAS Ctlgrs786205154
Max Magnitude0
ClinVar
Risk rs786205154(;)
Alt rs786205154(;)
Reference rs786205154(AACAG;AACAG)
Significance Pathogenic
Disease See cases LEUKEMIA ALL Thrombocytopenia Inborn genetic diseases
Variation info
Gene ETV6
CLNDBN See cases LEUKEMIA, ACUTE LYMPHOBLASTIC ALL Thrombocytopenia Inborn genetic diseases
Reversed 0
HGVS NC_000012.11:g.12038855_12038859delAACAG
CLNSRC
CLNACC RCV000170463.1, RCV000170466.1, RCV000170467.1, RCV000210685.1,