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

rs397508357

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508357(C;C)
Make rs397508357(C;G)
ReferenceGRCh38.p2 38.2/147
Chromosome7
Position117592419
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508357
ebirs397508357
HLIrs397508357
Exacrs397508357
Varsomers397508357
Maprs397508357
PheGenIrs397508357
hapmaprs397508357
1000 genomesrs397508357
hgdprs397508357
ensemblrs397508357
gopubmedrs397508357
geneviewrs397508357
scholarrs397508357
googlers397508357
pharmgkbrs397508357
gwascentralrs397508357
openSNPrs397508357
23andMers397508357
23andMe allrs397508357
SNP Nexus

SNPshotrs397508357
SNPdbers397508357
MSV3drs397508357
GWAS Ctlgrs397508357
Max Magnitude0
ClinVar
Risk rs397508357(A,C;A,C)
Alt rs397508357(A,C;A,C)
Reference rs397508357(G;G)
Significance Probable-Pathogenic
Disease Cystic fibrosis not provided
Variation info
Gene CFTR
CLNDBN Cystic fibrosis not provided
Reversed 0
HGVS NC_000007.13:g.117232473G>C; NC_000007.13:g.117232473G>T
CLNSRC
CLNACC RCV000046563.2, RCV000224113.1,