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

rs796052006

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796052006(A;A)
Make rs796052006(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position49457689
GeneMUT
is asnp
is mentioned by
dbSNPrs796052006
ebirs796052006
HLIrs796052006
Exacrs796052006
Varsomers796052006
Maprs796052006
PheGenIrs796052006
hapmaprs796052006
1000 genomesrs796052006
hgdprs796052006
ensemblrs796052006
gopubmedrs796052006
geneviewrs796052006
scholarrs796052006
googlers796052006
pharmgkbrs796052006
gwascentralrs796052006
openSNPrs796052006
23andMers796052006
23andMe allrs796052006
SNP Nexus

SNPshotrs796052006
SNPdbers796052006
MSV3drs796052006
GWAS Ctlgrs796052006
Max Magnitude0
ClinVar
Risk rs796052006(A;A)
Alt rs796052006(A;A)
Reference rs796052006(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene MUT
CLNDBN not provided
Reversed 1
HGVS NC_000006.11:g.49425402A>T
CLNSRC
CLNACC RCV000186057.1,