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rs17849598

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs17849598(C;T)
Make rs17849598(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271076
GeneHLA-C
is asnp
is mentioned by
dbSNPrs17849598
ebirs17849598
HLIrs17849598
Exacrs17849598
Varsomers17849598
Maprs17849598
PheGenIrs17849598
hapmaprs17849598
1000 genomesrs17849598
hgdprs17849598
ensemblrs17849598
gopubmedrs17849598
geneviewrs17849598
scholarrs17849598
googlers17849598
pharmgkbrs17849598
gwascentralrs17849598
openSNPrs17849598
23andMers17849598
23andMe allrs17849598
SNP Nexus

SNPshotrs17849598
SNPdbers17849598
MSV3drs17849598
GWAS Ctlgrs17849598
Max Magnitude0
ClinVar
Risk rs17849598(A,G,T;A,G,T)
Alt rs17849598(A,G,T;A,G,T)
Reference rs17849598(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31238853C>A; NC_000006.11:g.31238853C>G; NC_000006.11:g.31238853C>T
CLNSRC
CLNACC