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rs1050783

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1050783(A;A)
Make rs1050783(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position6145459
GeneF13A1
is asnp
is mentioned by
dbSNPrs1050783
dbSNP (old)rs1050783
ClinGenrs1050783
ebirs1050783
HLIrs1050783
Exacrs1050783
Varsomers1050783
Maprs1050783
PheGenIrs1050783
Biobankrs1050783
1000 genomesrs1050783
hgdprs1050783
ensemblrs1050783
gopubmedrs1050783
geneviewrs1050783
scholarrs1050783
googlers1050783
pharmgkbrs1050783
gwascentralrs1050783
openSNPrs1050783
23andMers1050783
23andMe allrs1050783
SNP Nexus

SNPshotrs1050783
SNPdbers1050783
MSV3drs1050783
GWAS Ctlgrs1050783
GMAF0.1488
Max Magnitude0
? (A;A) (A;G) (G;G) 28
[PMID 24159917OA-icon.png] Gastrointestinal stromal tumors: a case-only analysis of single nucleotide polymorphisms and somatic mutations


ClinVar
Risk rs1050783(A;A)
Alt rs1050783(A;A)
Reference Rs1050783(G;G)
Significance Probable-non-pathogenic
Disease Factor xiii
Variation info
Gene F13A1
CLNDBN Factor xiii, a subunit, deficiency of
Reversed 1
HGVS NC_000006.11:g.6145692C>T
CLNSRC
CLNACC RCV000288686.1,