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rs199422291

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199422291(A;A)
Make rs199422291(A;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position1294456
GeneTERT
is asnp
is mentioned by
dbSNPrs199422291
dbSNP (classic)rs199422291
ClinGenrs199422291
ebirs199422291
HLIrs199422291
Exacrs199422291
Gnomadrs199422291
Varsomers199422291
LitVarrs199422291
Maprs199422291
PheGenIrs199422291
Biobankrs199422291
1000 genomesrs199422291
hgdprs199422291
ensemblrs199422291
geneviewrs199422291
scholarrs199422291
googlers199422291
pharmgkbrs199422291
gwascentralrs199422291
openSNPrs199422291
23andMers199422291
SNPshotrs199422291
SNPdbers199422291
MSV3drs199422291
GWAS Ctlgrs199422291
Max Magnitude0
ClinVar
Risk rs199422291(A;A)
Alt rs199422291(A;A)
Reference Rs199422291(G;G)
Significance Pathogenic
Disease Idiopathic fibrosing alveolitis not provided
Variation info
Gene TERT
CLNDBN Idiopathic fibrosing alveolitis, chronic form not provided
Reversed 1
HGVS NC_000005.9:g.1294571C>T
CLNSRC ClinVar GeneReviews
CLNACC RCV000032397.1, RCV000256024.1,