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rs141686314

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs141686314(C;T)
Make rs141686314(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position169764833
GeneTERC
is asnp
is mentioned by
dbSNPrs141686314
ebirs141686314
HLIrs141686314
Exacrs141686314
Varsomers141686314
Maprs141686314
PheGenIrs141686314
hapmaprs141686314
1000 genomesrs141686314
hgdprs141686314
ensemblrs141686314
gopubmedrs141686314
geneviewrs141686314
scholarrs141686314
googlers141686314
pharmgkbrs141686314
gwascentralrs141686314
openSNPrs141686314
23andMers141686314
23andMe allrs141686314
SNP Nexus

SNPshotrs141686314
SNPdbers141686314
MSV3drs141686314
GWAS Ctlgrs141686314
GMAF0.003673
Max Magnitude0
ClinVar
Risk rs141686314(T;T)
Alt rs141686314(T;T)
Reference rs141686314(C;C)
Significance Pathogenic
Disease Dyskeratosis congenita autosomal dominant not provided
Variation info
Gene TERC
CLNDBN Dyskeratosis congenita autosomal dominant not provided
Reversed 0
HGVS NC_000003.11:g.169482621C>T
CLNSRC ClinVar GeneReviews
CLNACC RCV000032566.1, RCV000224681.1,