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rs374705585

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 3 cystic fibrosis carrier
Make rs374705585(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117667091
GeneCFTR
is asnp
is mentioned by
dbSNPrs374705585
ebirs374705585
HLIrs374705585
Exacrs374705585
Varsomers374705585
Maprs374705585
PheGenIrs374705585
hapmaprs374705585
1000 genomesrs374705585
hgdprs374705585
ensemblrs374705585
gopubmedrs374705585
geneviewrs374705585
scholarrs374705585
googlers374705585
pharmgkbrs374705585
gwascentralrs374705585
openSNPrs374705585
23andMers374705585
23andMe allrs374705585
SNP Nexus

SNPshotrs374705585
SNPdbers374705585
MSV3drs374705585
GWAS Ctlgrs374705585
Max Magnitude3
ClinVar
Risk rs374705585(T;T)
Alt rs374705585(T;T)
Reference rs374705585(C;C)
Significance Pathogenic
Disease Cystic fibrosis not provided
Variation info
Gene CFTR
CLNDBN Cystic fibrosis not provided
Reversed 0
HGVS NC_000007.13:g.117307145C>T
CLNSRC HGMD
CLNACC RCV000047135.3, RCV000079008.3,