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rs766420051

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs766420051(C;G)
Make rs766420051(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome6
Position49456165
GeneMUT
is asnp
is mentioned by
dbSNPrs766420051
ebirs766420051
HLIrs766420051
Exacrs766420051
Varsomers766420051
Maprs766420051
PheGenIrs766420051
hapmaprs766420051
1000 genomesrs766420051
hgdprs766420051
ensemblrs766420051
gopubmedrs766420051
geneviewrs766420051
scholarrs766420051
googlers766420051
pharmgkbrs766420051
gwascentralrs766420051
openSNPrs766420051
23andMers766420051
23andMe allrs766420051
SNP Nexus

SNPshotrs766420051
SNPdbers766420051
MSV3drs766420051
GWAS Ctlgrs766420051
Max Magnitude0
ClinVar
Risk rs766420051(G;G)
Alt rs766420051(G;G)
Reference rs766420051(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene MUT
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.49423878C>A
CLNSRC
CLNACC RCV000186058.1,