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rs796052003

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052003(C;C)
Make rs796052003(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position49451474
GeneMUT
is asnp
is mentioned by
dbSNPrs796052003
ebirs796052003
HLIrs796052003
Exacrs796052003
Varsomers796052003
Maprs796052003
PheGenIrs796052003
hapmaprs796052003
1000 genomesrs796052003
hgdprs796052003
ensemblrs796052003
gopubmedrs796052003
geneviewrs796052003
scholarrs796052003
googlers796052003
pharmgkbrs796052003
gwascentralrs796052003
openSNPrs796052003
23andMers796052003
23andMe allrs796052003
SNP Nexus

SNPshotrs796052003
SNPdbers796052003
MSV3drs796052003
GWAS Ctlgrs796052003
Max Magnitude0
ClinVar
Risk rs796052003(C;C)
Alt rs796052003(C;C)
Reference rs796052003(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MUT
CLNDBN not provided
Reversed 1
HGVS NC_000006.11:g.49419187C>G
CLNSRC
CLNACC RCV000186048.1,