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

rs281860570

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281860570(A;A)
Make rs281860570(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270247
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860570
ebirs281860570
HLIrs281860570
Exacrs281860570
Varsomers281860570
Maprs281860570
PheGenIrs281860570
hapmaprs281860570
1000 genomesrs281860570
hgdprs281860570
ensemblrs281860570
gopubmedrs281860570
geneviewrs281860570
scholarrs281860570
googlers281860570
pharmgkbrs281860570
gwascentralrs281860570
openSNPrs281860570
23andMers281860570
23andMe allrs281860570
SNP Nexus

SNPshotrs281860570
SNPdbers281860570
MSV3drs281860570
GWAS Ctlgrs281860570
Max Magnitude0
ClinVar
Risk rs281860570(A;A)
Alt rs281860570(A;A)
Reference rs281860570(G;G)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238024C>T
CLNSRC
CLNACC