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rs104893973

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs104893973(C;C)
Make rs104893973(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position137206249
GeneIFNGR1
is asnp
is mentioned by
dbSNPrs104893973
ebirs104893973
HLIrs104893973
Exacrs104893973
Varsomers104893973
Maprs104893973
PheGenIrs104893973
hapmaprs104893973
1000 genomesrs104893973
hgdprs104893973
ensemblrs104893973
gopubmedrs104893973
geneviewrs104893973
scholarrs104893973
googlers104893973
pharmgkbrs104893973
gwascentralrs104893973
openSNPrs104893973
23andMers104893973
23andMe allrs104893973
SNP Nexus

SNPshotrs104893973
SNPdbers104893973
MSV3drs104893973
GWAS Ctlgrs104893973
Max Magnitude0
OMIM107470
Desc
Variant0003
Relatedalso
ClinVar
Risk rs104893973(C;C)
Alt rs104893973(C;C)
Reference rs104893973(T;T)
Significance Other
Disease Disseminated atypical mycobacterial infection Mycobacterium tuberculosis
Variation info
Gene IFNGR1
CLNDBN Disseminated atypical mycobacterial infection Mycobacterium tuberculosis, susceptibility to
Reversed 1
HGVS NC_000006.11:g.137527386A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000019539.30, RCV000144034.3,