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rs796052007

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796052007(C;C)
Make rs796052007(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position49456149
GeneMUT
is asnp
is mentioned by
dbSNPrs796052007
ebirs796052007
HLIrs796052007
Exacrs796052007
Varsomers796052007
Maprs796052007
PheGenIrs796052007
hapmaprs796052007
1000 genomesrs796052007
hgdprs796052007
ensemblrs796052007
gopubmedrs796052007
geneviewrs796052007
scholarrs796052007
googlers796052007
pharmgkbrs796052007
gwascentralrs796052007
openSNPrs796052007
23andMers796052007
23andMe allrs796052007
SNP Nexus

SNPshotrs796052007
SNPdbers796052007
MSV3drs796052007
GWAS Ctlgrs796052007
Max Magnitude0
ClinVar
Risk rs796052007(C;C)
Alt rs796052007(C;C)
Reference rs796052007(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene MUT
CLNDBN not provided
Reversed 1
HGVS NC_000006.11:g.49423862A>G
CLNSRC
CLNACC RCV000186059.2,