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rs863225129

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863225129(A;A)
Make rs863225129(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position63687936
GeneRTEL1, RTEL1-TNFRSF6B
is asnp
is mentioned by
dbSNPrs863225129
dbSNP (classic)rs863225129
ClinGenrs863225129
ebirs863225129
HLIrs863225129
Exacrs863225129
Gnomadrs863225129
Varsomers863225129
LitVarrs863225129
Maprs863225129
PheGenIrs863225129
Biobankrs863225129
1000 genomesrs863225129
hgdprs863225129
ensemblrs863225129
geneviewrs863225129
scholarrs863225129
googlers863225129
pharmgkbrs863225129
gwascentralrs863225129
openSNPrs863225129
23andMers863225129
SNPshotrs863225129
SNPdbers863225129
MSV3drs863225129
GWAS Ctlgrs863225129
Max Magnitude0
ClinVar
Risk rs863225129(A;A)
Alt rs863225129(A;A)
Reference Rs863225129(G;G)
Significance Pathogenic
Disease Idiopathic fibrosing alveolitis
Variation info
Gene RTEL1-TNFRSF6B RTEL1
CLNDBN Idiopathic fibrosing alveolitis, chronic form
Reversed 0
HGVS NC_000020.10:g.62319289G>A
CLNSRC
CLNACC RCV000201560.1,