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rs869312855

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs869312855(-;-)
Make rs869312855(-;T)
Make rs869312855(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position63678185
GeneRTEL1, RTEL1-TNFRSF6B
is asnp
is mentioned by
dbSNPrs869312855
ebirs869312855
HLIrs869312855
Exacrs869312855
Varsomers869312855
Maprs869312855
PheGenIrs869312855
hapmaprs869312855
1000 genomesrs869312855
hgdprs869312855
ensemblrs869312855
gopubmedrs869312855
geneviewrs869312855
scholarrs869312855
googlers869312855
pharmgkbrs869312855
gwascentralrs869312855
openSNPrs869312855
23andMers869312855
23andMe allrs869312855
SNP Nexus

SNPshotrs869312855
SNPdbers869312855
MSV3drs869312855
GWAS Ctlgrs869312855
Max Magnitude0
ClinVar
Risk rs869312855(T;T)
Alt rs869312855(T;T)
Reference rs869312855(;)
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.62309538dupT
CLNSRC
CLNACC RCV000201698.1,