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rs137854490

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Make rs137854490(CT;TA)
Make rs137854490(TA;TA)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154765468
GeneDKC1
is asnp
is mentioned by
dbSNPrs137854490
ebirs137854490
HLIrs137854490
Exacrs137854490
Varsomers137854490
Maprs137854490
PheGenIrs137854490
hapmaprs137854490
1000 genomesrs137854490
hgdprs137854490
ensemblrs137854490
gopubmedrs137854490
geneviewrs137854490
scholarrs137854490
googlers137854490
pharmgkbrs137854490
gwascentralrs137854490
openSNPrs137854490
23andMers137854490
23andMe allrs137854490
SNP Nexus

SNPshotrs137854490
SNPdbers137854490
MSV3drs137854490
GWAS Ctlgrs137854490
Max Magnitude0
OMIM300126
Desc
Variant0004
Relatedalso
ClinVar
Risk rs137854490(TA;TA)
Alt rs137854490(TA;TA)
Reference rs137854490(CT;CT)
Significance Untested
Disease Dyskeratosis congenita X-linked
Variation info
Gene DKC1
CLNDBN Dyskeratosis congenita X-linked
Reversed 0
HGVS NC_000023.10:g.153993743_153993744delCTinsTA
CLNSRC OMIM Allelic Variant
CLNACC SCV000032575.1, SCV000032575.1,