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rs104893974

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104893974(A;A)
Make rs104893974(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position137206279
GeneIFNGR1
is asnp
is mentioned by
dbSNPrs104893974
ebirs104893974
HLIrs104893974
Exacrs104893974
Varsomers104893974
Maprs104893974
PheGenIrs104893974
hapmaprs104893974
1000 genomesrs104893974
hgdprs104893974
ensemblrs104893974
gopubmedrs104893974
geneviewrs104893974
scholarrs104893974
googlers104893974
pharmgkbrs104893974
gwascentralrs104893974
openSNPrs104893974
23andMers104893974
23andMe allrs104893974
SNP Nexus

SNPshotrs104893974
SNPdbers104893974
MSV3drs104893974
GWAS Ctlgrs104893974
Max Magnitude0
OMIM107470
Desc
Variant0008
Relatedalso
ClinVar
Risk rs104893974(A;A)
Alt rs104893974(A;A)
Reference rs104893974(G;G)
Significance Pathogenic
Disease Disseminated atypical mycobacterial infection
Variation info
Gene IFNGR1
CLNDBN Disseminated atypical mycobacterial infection
Reversed 1
HGVS NC_000006.11:g.137527416C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000019545.31,