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rs786205512

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205512(A;A)
Make rs786205512(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome18
Position49286433
GeneDYM
is asnp
is mentioned by
dbSNPrs786205512
ebirs786205512
HLIrs786205512
Exacrs786205512
Varsomers786205512
Maprs786205512
PheGenIrs786205512
hapmaprs786205512
1000 genomesrs786205512
hgdprs786205512
ensemblrs786205512
gopubmedrs786205512
geneviewrs786205512
scholarrs786205512
googlers786205512
pharmgkbrs786205512
gwascentralrs786205512
openSNPrs786205512
23andMers786205512
23andMe allrs786205512
SNP Nexus

SNPshotrs786205512
SNPdbers786205512
MSV3drs786205512
GWAS Ctlgrs786205512
Max Magnitude0
ClinVar
Risk rs786205512(A;A)
Alt rs786205512(A;A)
Reference rs786205512(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DYM
CLNDBN not provided
Reversed 1
HGVS NC_000018.9:g.46812803C>T
CLNSRC
CLNACC RCV000171273.1,