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rs1655895

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1655895(C;C)
Make rs1655895(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29944740
GeneHLA-A
is asnp
is mentioned by
dbSNPrs1655895
dbSNP (classic)rs1655895
ClinGenrs1655895
ebirs1655895
HLIrs1655895
Exacrs1655895
Gnomadrs1655895
Varsomers1655895
LitVarrs1655895
Maprs1655895
PheGenIrs1655895
Biobankrs1655895
1000 genomesrs1655895
hgdprs1655895
ensemblrs1655895
geneviewrs1655895
scholarrs1655895
googlers1655895
pharmgkbrs1655895
gwascentralrs1655895
openSNPrs1655895
23andMers1655895
SNPshotrs1655895
SNPdbers1655895
MSV3drs1655895
GWAS Ctlgrs1655895
GMAF0.09871
Max Magnitude0
ClinVar
Risk rs1655895(C;C)
Alt rs1655895(C;C)
Reference Rs1655895(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29912517T; NC_000006.11:g.29912517T>C
CLNSRC
CLNACC