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

rs397508734

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508734(A;A)
Make rs397508734(A;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117534275
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508734
ebirs397508734
HLIrs397508734
Exacrs397508734
Varsomers397508734
Maprs397508734
PheGenIrs397508734
hapmaprs397508734
1000 genomesrs397508734
hgdprs397508734
ensemblrs397508734
gopubmedrs397508734
geneviewrs397508734
scholarrs397508734
googlers397508734
pharmgkbrs397508734
gwascentralrs397508734
openSNPrs397508734
23andMers397508734
23andMe allrs397508734
SNP Nexus

SNPshotrs397508734
SNPdbers397508734
MSV3drs397508734
GWAS Ctlgrs397508734
Max Magnitude0
ClinVar
Risk rs397508734(A;A)
Alt rs397508734(A;A)
Reference rs397508734(G;G)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117174329G>A
CLNSRC ClinVar
CLNACC RCV000047165.2,