Have questions? Visit https://www.reddit.com/r/SNPedia

rs267607026

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267607026(A;A)
Make rs267607026(A;C)
ReferenceGRCh38 38.1/141
Chromosome21
Position34880598
GeneRUNX1
is asnp
is mentioned by
dbSNPrs267607026
ebirs267607026
HLIrs267607026
Exacrs267607026
Varsomers267607026
Maprs267607026
PheGenIrs267607026
hapmaprs267607026
1000 genomesrs267607026
hgdprs267607026
ensemblrs267607026
gopubmedrs267607026
geneviewrs267607026
scholarrs267607026
googlers267607026
pharmgkbrs267607026
gwascentralrs267607026
openSNPrs267607026
23andMers267607026
23andMe allrs267607026
SNP Nexus

SNPshotrs267607026
SNPdbers267607026
MSV3drs267607026
GWAS Ctlgrs267607026
Max Magnitude0
ClinVar
Risk rs267607026(A;A)
Alt rs267607026(A;A)
Reference rs267607026(C;C)
Significance Pathogenic
Disease Familial platelet disorder with associated myeloid malignancy
Variation info
Gene RUNX1
CLNDBN Familial platelet disorder with associated myeloid malignancy
Reversed 1
HGVS NC_000021.8:g.36252895G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000015558.26,