Have questions? Visit https://www.reddit.com/r/SNPedia

rs397508669

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
(-;T) 3 carrier of a cystic fibrosis allele
Make rs397508669(-;-)
Make rs397508669(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117664810
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508669
ebirs397508669
HLIrs397508669
Exacrs397508669
Varsomers397508669
Maprs397508669
PheGenIrs397508669
hapmaprs397508669
1000 genomesrs397508669
hgdprs397508669
ensemblrs397508669
gopubmedrs397508669
geneviewrs397508669
scholarrs397508669
googlers397508669
pharmgkbrs397508669
gwascentralrs397508669
openSNPrs397508669
23andMers397508669
23andMe allrs397508669
SNP Nexus

SNPshotrs397508669
SNPdbers397508669
MSV3drs397508669
GWAS Ctlgrs397508669
Max Magnitude3
ClinVar
Risk rs397508669(T;T)
Alt rs397508669(T;T)
Reference rs397508669(;)
Significance Pathogenic
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117304864dupT
CLNSRC CFTR2
CLNACC RCV000047069.3,