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rs796052004

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796052004(A;G)
Make rs796052004(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position49440277
GeneMUT
is asnp
is mentioned by
dbSNPrs796052004
ebirs796052004
HLIrs796052004
Exacrs796052004
Varsomers796052004
Maprs796052004
PheGenIrs796052004
hapmaprs796052004
1000 genomesrs796052004
hgdprs796052004
ensemblrs796052004
gopubmedrs796052004
geneviewrs796052004
scholarrs796052004
googlers796052004
pharmgkbrs796052004
gwascentralrs796052004
openSNPrs796052004
23andMers796052004
23andMe allrs796052004
SNP Nexus

SNPshotrs796052004
SNPdbers796052004
MSV3drs796052004
GWAS Ctlgrs796052004
Max Magnitude0
ClinVar
Risk rs796052004(G;G)
Alt rs796052004(G;G)
Reference rs796052004(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene MUT
CLNDBN not provided
Reversed 1
HGVS NC_000006.11:g.49407990T>C
CLNSRC
CLNACC RCV000186051.1,