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

rs144830948

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs144830948(A;A)
Make rs144830948(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome21
Position46132050
GeneCOL6A2
is asnp
is mentioned by
dbSNPrs144830948
ebirs144830948
HLIrs144830948
Exacrs144830948
Varsomers144830948
Maprs144830948
PheGenIrs144830948
hapmaprs144830948
1000 genomesrs144830948
hgdprs144830948
ensemblrs144830948
gopubmedrs144830948
geneviewrs144830948
scholarrs144830948
googlers144830948
pharmgkbrs144830948
gwascentralrs144830948
openSNPrs144830948
23andMers144830948
23andMe allrs144830948
SNP Nexus

SNPshotrs144830948
SNPdbers144830948
MSV3drs144830948
GWAS Ctlgrs144830948
Max Magnitude0
ClinVar
Risk rs144830948(A;A)
Alt rs144830948(A;A)
Reference rs144830948(G;G)
Significance Probable-non-pathogenic
Disease not specified
Variation info
Gene COL6A2
CLNDBN not specified
Reversed 0
HGVS NC_000021.8:g.47551964G>A
CLNSRC
CLNACC RCV000149936.2,