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rs199422289

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199422289(C;T)
Make rs199422289(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position1294893
GeneTERT
is asnp
is mentioned by
dbSNPrs199422289
dbSNP (classic)rs199422289
ClinGenrs199422289
ebirs199422289
HLIrs199422289
Exacrs199422289
Gnomadrs199422289
Varsomers199422289
LitVarrs199422289
Maprs199422289
PheGenIrs199422289
Biobankrs199422289
1000 genomesrs199422289
hgdprs199422289
ensemblrs199422289
geneviewrs199422289
scholarrs199422289
googlers199422289
pharmgkbrs199422289
gwascentralrs199422289
openSNPrs199422289
23andMers199422289
SNPshotrs199422289
SNPdbers199422289
MSV3drs199422289
GWAS Ctlgrs199422289
Max Magnitude0
ClinVar
Risk rs199422289(T;T)
Alt rs199422289(T;T)
Reference Rs199422289(C;C)
Significance Pathogenic
Disease Idiopathic fibrosing alveolitis
Variation info
Gene TERT
CLNDBN Idiopathic fibrosing alveolitis, chronic form
Reversed 1
HGVS NC_000005.9:g.1295008G>A
CLNSRC ClinVar GeneReviews
CLNACC RCV000032401.1,