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rs863225130

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863225130(G;G)
Make rs863225130(G;T)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position63688161
GeneRTEL1, RTEL1-TNFRSF6B
is asnp
is mentioned by
dbSNPrs863225130
ebirs863225130
HLIrs863225130
Exacrs863225130
Varsomers863225130
Maprs863225130
PheGenIrs863225130
hapmaprs863225130
1000 genomesrs863225130
hgdprs863225130
ensemblrs863225130
gopubmedrs863225130
geneviewrs863225130
scholarrs863225130
googlers863225130
pharmgkbrs863225130
gwascentralrs863225130
openSNPrs863225130
23andMers863225130
23andMe allrs863225130
SNP Nexus

SNPshotrs863225130
SNPdbers863225130
MSV3drs863225130
GWAS Ctlgrs863225130
Max Magnitude0
ClinVar
Risk rs863225130(G;G)
Alt rs863225130(G;G)
Reference Rs863225130(T;T)
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.62319514T>G
CLNSRC
CLNACC RCV000201743.1,