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

rs148059981

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs148059981(C;T)
Make rs148059981(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome18
Position49363233
GeneDYM
is asnp
is mentioned by
dbSNPrs148059981
ebirs148059981
HLIrs148059981
Exacrs148059981
Varsomers148059981
Maprs148059981
PheGenIrs148059981
hapmaprs148059981
1000 genomesrs148059981
hgdprs148059981
ensemblrs148059981
gopubmedrs148059981
geneviewrs148059981
scholarrs148059981
googlers148059981
pharmgkbrs148059981
gwascentralrs148059981
openSNPrs148059981
23andMers148059981
23andMe allrs148059981
SNP Nexus

SNPshotrs148059981
SNPdbers148059981
MSV3drs148059981
GWAS Ctlgrs148059981
Max Magnitude0
ClinVar
Risk rs148059981(T;T)
Alt rs148059981(T;T)
Reference rs148059981(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DYM
CLNDBN not provided
Reversed 0
HGVS NC_000018.9:g.46889603C>T
CLNSRC
CLNACC RCV000171274.1,