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rs779212460

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs779212460(C;T)
Make rs779212460(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position123725955
GeneMYLK
is asnp
is mentioned by
dbSNPrs779212460
ebirs779212460
HLIrs779212460
Exacrs779212460
Varsomers779212460
Maprs779212460
PheGenIrs779212460
hapmaprs779212460
1000 genomesrs779212460
hgdprs779212460
ensemblrs779212460
gopubmedrs779212460
geneviewrs779212460
scholarrs779212460
googlers779212460
pharmgkbrs779212460
gwascentralrs779212460
openSNPrs779212460
23andMers779212460
23andMe allrs779212460
SNP Nexus

SNPshotrs779212460
SNPdbers779212460
MSV3drs779212460
GWAS Ctlgrs779212460
Max Magnitude0
ClinVar
Risk rs779212460(T;T)
Alt rs779212460(T;T)
Reference rs779212460(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene MYLK
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.123444802C>T
CLNSRC
CLNACC RCV000182570.1,