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rs796052002

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052002(C;T)
Make rs796052002(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position49453686
GeneMUT
is asnp
is mentioned by
dbSNPrs796052002
ebirs796052002
HLIrs796052002
Exacrs796052002
Varsomers796052002
Maprs796052002
PheGenIrs796052002
hapmaprs796052002
1000 genomesrs796052002
hgdprs796052002
ensemblrs796052002
gopubmedrs796052002
geneviewrs796052002
scholarrs796052002
googlers796052002
pharmgkbrs796052002
gwascentralrs796052002
openSNPrs796052002
23andMers796052002
23andMe allrs796052002
SNP Nexus

SNPshotrs796052002
SNPdbers796052002
MSV3drs796052002
GWAS Ctlgrs796052002
Max Magnitude0
ClinVar
Risk rs796052002(T;T)
Alt rs796052002(T;T)
Reference rs796052002(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene MUT
CLNDBN not provided
Reversed 1
HGVS NC_000006.11:g.49421399G>A
CLNSRC
CLNACC RCV000186044.1,