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rs786205513

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786205513(C;G)
Make rs786205513(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome18
Position49379680
GeneDYM
is asnp
is mentioned by
dbSNPrs786205513
ebirs786205513
HLIrs786205513
Exacrs786205513
Varsomers786205513
Maprs786205513
PheGenIrs786205513
hapmaprs786205513
1000 genomesrs786205513
hgdprs786205513
ensemblrs786205513
gopubmedrs786205513
geneviewrs786205513
scholarrs786205513
googlers786205513
pharmgkbrs786205513
gwascentralrs786205513
openSNPrs786205513
23andMers786205513
23andMe allrs786205513
SNP Nexus

SNPshotrs786205513
SNPdbers786205513
MSV3drs786205513
GWAS Ctlgrs786205513
Max Magnitude0
ClinVar
Risk rs786205513(G;G)
Alt rs786205513(G;G)
Reference rs786205513(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DYM
CLNDBN not provided
Reversed 1
HGVS NC_000018.9:g.46906050G>C
CLNSRC
CLNACC RCV000171275.1,