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rs373002889

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;T) 3 cystic fibrosis carrier
(T;T) 0 common in clinvar


Make rs373002889(C;C)
ReferenceGRCh38 38.1/141
Chromosome7
Position117627502
GeneCFTR
is asnp
is mentioned by
dbSNPrs373002889
ebirs373002889
HLIrs373002889
Exacrs373002889
Varsomers373002889
Maprs373002889
PheGenIrs373002889
hapmaprs373002889
1000 genomesrs373002889
hgdprs373002889
ensemblrs373002889
gopubmedrs373002889
geneviewrs373002889
scholarrs373002889
googlers373002889
pharmgkbrs373002889
gwascentralrs373002889
openSNPrs373002889
23andMers373002889
23andMe allrs373002889
SNP Nexus

SNPshotrs373002889
SNPdbers373002889
MSV3drs373002889
GWAS Ctlgrs373002889
Max Magnitude3
ClinVar
Risk rs373002889(C;C)
Alt rs373002889(C;C)
Reference rs373002889(T;T)
Significance Pathogenic
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117267556T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000007649.3,