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

rs770873593

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs770873593(C;T)
Make rs770873593(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome6
Position7580388
GeneDSP
is asnp
is mentioned by
dbSNPrs770873593
ebirs770873593
HLIrs770873593
Exacrs770873593
Varsomers770873593
Maprs770873593
PheGenIrs770873593
hapmaprs770873593
1000 genomesrs770873593
hgdprs770873593
ensemblrs770873593
gopubmedrs770873593
geneviewrs770873593
scholarrs770873593
googlers770873593
pharmgkbrs770873593
gwascentralrs770873593
openSNPrs770873593
23andMers770873593
23andMe allrs770873593
SNP Nexus

SNPshotrs770873593
SNPdbers770873593
MSV3drs770873593
GWAS Ctlgrs770873593
Max Magnitude0
ClinVar
Risk rs770873593(T;T)
Alt rs770873593(T;T)
Reference rs770873593(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene DSP
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.7580621C>T
CLNSRC
CLNACC RCV000181321.1,