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rs779637525

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs779637525(G;T)
Make rs779637525(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position31826918
GeneMYLK2
is asnp
is mentioned by
dbSNPrs779637525
ebirs779637525
HLIrs779637525
Exacrs779637525
Varsomers779637525
Maprs779637525
PheGenIrs779637525
hapmaprs779637525
1000 genomesrs779637525
hgdprs779637525
ensemblrs779637525
gopubmedrs779637525
geneviewrs779637525
scholarrs779637525
googlers779637525
pharmgkbrs779637525
gwascentralrs779637525
openSNPrs779637525
23andMers779637525
23andMe allrs779637525
SNP Nexus

SNPshotrs779637525
SNPdbers779637525
MSV3drs779637525
GWAS Ctlgrs779637525
Max Magnitude0
ClinVar
Risk rs779637525(T;T)
Alt rs779637525(T;T)
Reference rs779637525(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene MYLK2
CLNDBN not provided
Reversed 0
HGVS NC_000020.10:g.30414721G>T
CLNSRC
CLNACC RCV000183563.1,