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rs369419645

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs369419645(C;T)
Make rs369419645(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome20
Position63688312
GeneRTEL1, RTEL1-TNFRSF6B
is asnp
is mentioned by
dbSNPrs369419645
dbSNP (classic)rs369419645
ClinGenrs369419645
ebirs369419645
HLIrs369419645
Exacrs369419645
Gnomadrs369419645
Varsomers369419645
LitVarrs369419645
Maprs369419645
PheGenIrs369419645
Biobankrs369419645
1000 genomesrs369419645
hgdprs369419645
ensemblrs369419645
geneviewrs369419645
scholarrs369419645
googlers369419645
pharmgkbrs369419645
gwascentralrs369419645
openSNPrs369419645
23andMers369419645
SNPshotrs369419645
SNPdbers369419645
MSV3drs369419645
GWAS Ctlgrs369419645
Max Magnitude0
ClinVar
Risk rs369419645(T;T)
Alt rs369419645(T;T)
Reference Rs369419645(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RTEL1-TNFRSF6B RTEL1
CLNDBN not provided
Reversed 0
HGVS NC_000020.10:g.62319665C>T
CLNSRC
CLNACC RCV000478358.1,