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rs796052005

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796052005(A;G)
Make rs796052005(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position49459138
GeneMUT
is asnp
is mentioned by
dbSNPrs796052005
ebirs796052005
HLIrs796052005
Exacrs796052005
Varsomers796052005
Maprs796052005
PheGenIrs796052005
hapmaprs796052005
1000 genomesrs796052005
hgdprs796052005
ensemblrs796052005
gopubmedrs796052005
geneviewrs796052005
scholarrs796052005
googlers796052005
pharmgkbrs796052005
gwascentralrs796052005
openSNPrs796052005
23andMers796052005
23andMe allrs796052005
SNP Nexus

SNPshotrs796052005
SNPdbers796052005
MSV3drs796052005
GWAS Ctlgrs796052005
Max Magnitude0
ClinVar
Risk rs796052005(G;G)
Alt rs796052005(G;G)
Reference rs796052005(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene MUT
CLNDBN not provided
Reversed 1
HGVS NC_000006.11:g.49426851T>C
CLNSRC
CLNACC RCV000186053.1,