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rs146444598

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GGA;GGA) 0 common in clinvar
Make rs146444598(-;-)
Make rs146444598(-;GGA)
ReferenceGRCh38 38.1/141
Chromosome6
Position29944451
GeneHLA-A
is asnp
is mentioned by
dbSNPrs146444598
ebirs146444598
HLIrs146444598
Exacrs146444598
Varsomers146444598
Maprs146444598
PheGenIrs146444598
hapmaprs146444598
1000 genomesrs146444598
hgdprs146444598
ensemblrs146444598
gopubmedrs146444598
geneviewrs146444598
scholarrs146444598
googlers146444598
pharmgkbrs146444598
gwascentralrs146444598
openSNPrs146444598
23andMers146444598
23andMe allrs146444598
SNP Nexus

SNPshotrs146444598
SNPdbers146444598
MSV3drs146444598
GWAS Ctlgrs146444598
Merged fromRs45473895
Max Magnitude0
ClinVar
Risk rs146444598(;)
Alt rs146444598(;)
Reference rs146444598(GGA;GGA)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29912228_29912230delGGA
CLNSRC
CLNACC