Have questions? Visit https://www.reddit.com/r/SNPedia

rs786205511

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205511(A;A)
Make rs786205511(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome18
Position49097401
GeneDYM
is asnp
is mentioned by
dbSNPrs786205511
ebirs786205511
HLIrs786205511
Exacrs786205511
Varsomers786205511
Maprs786205511
PheGenIrs786205511
hapmaprs786205511
1000 genomesrs786205511
hgdprs786205511
ensemblrs786205511
gopubmedrs786205511
geneviewrs786205511
scholarrs786205511
googlers786205511
pharmgkbrs786205511
gwascentralrs786205511
openSNPrs786205511
23andMers786205511
23andMe allrs786205511
SNP Nexus

SNPshotrs786205511
SNPdbers786205511
MSV3drs786205511
GWAS Ctlgrs786205511
Max Magnitude0
ClinVar
Risk rs786205511(A;A)
Alt rs786205511(A;A)
Reference rs786205511(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DYM
CLNDBN not provided
Reversed 1
HGVS NC_000018.9:g.46623771C>T
CLNSRC
CLNACC RCV000171271.1,