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rs796065051

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796065051(C;T)
Make rs796065051(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position50319953
GeneBRD7
is asnp
is mentioned by
dbSNPrs796065051
ebirs796065051
HLIrs796065051
Exacrs796065051
Varsomers796065051
Maprs796065051
PheGenIrs796065051
hapmaprs796065051
1000 genomesrs796065051
hgdprs796065051
ensemblrs796065051
gopubmedrs796065051
geneviewrs796065051
scholarrs796065051
googlers796065051
pharmgkbrs796065051
gwascentralrs796065051
openSNPrs796065051
23andMers796065051
23andMe allrs796065051
SNP Nexus

SNPshotrs796065051
SNPdbers796065051
MSV3drs796065051
GWAS Ctlgrs796065051
Max Magnitude0
ClinVar
Risk rs796065051(T;T)
Alt rs796065051(T;T)
Reference rs796065051(C;C)
Significance Probable-Pathogenic
Disease malignant granular cell tumor
Variation info
Gene BRD7
CLNDBN malignant granular cell tumor
Reversed 1
HGVS NC_000016.9:g.50353864G>A
CLNSRC
CLNACC RCV000190398.2,