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rs777031588

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs777031588(C;C)
Make rs777031588(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome6
Position49451724
GeneMUT
is asnp
is mentioned by
dbSNPrs777031588
ebirs777031588
HLIrs777031588
Exacrs777031588
Varsomers777031588
Maprs777031588
PheGenIrs777031588
hapmaprs777031588
1000 genomesrs777031588
hgdprs777031588
ensemblrs777031588
gopubmedrs777031588
geneviewrs777031588
scholarrs777031588
googlers777031588
pharmgkbrs777031588
gwascentralrs777031588
openSNPrs777031588
23andMers777031588
23andMe allrs777031588
SNP Nexus

SNPshotrs777031588
SNPdbers777031588
MSV3drs777031588
GWAS Ctlgrs777031588
Max Magnitude0
ClinVar
Risk rs777031588(C;C)
Alt rs777031588(C;C)
Reference rs777031588(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MUT
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.49419437T>C
CLNSRC
CLNACC RCV000186045.1,