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rs771414481

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs771414481(A;A)
Make rs771414481(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome18
Position49258463
GeneDYM
is asnp
is mentioned by
dbSNPrs771414481
ebirs771414481
HLIrs771414481
Exacrs771414481
Varsomers771414481
Maprs771414481
PheGenIrs771414481
hapmaprs771414481
1000 genomesrs771414481
hgdprs771414481
ensemblrs771414481
gopubmedrs771414481
geneviewrs771414481
scholarrs771414481
googlers771414481
pharmgkbrs771414481
gwascentralrs771414481
openSNPrs771414481
23andMers771414481
23andMe allrs771414481
SNP Nexus

SNPshotrs771414481
SNPdbers771414481
MSV3drs771414481
GWAS Ctlgrs771414481
Max Magnitude0
ClinVar
Risk rs771414481(A;A)
Alt rs771414481(A;A)
Reference rs771414481(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DYM
CLNDBN not provided
Reversed 0
HGVS NC_000018.9:g.46784833G>A
CLNSRC
CLNACC RCV000171272.1,