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

rs397508456

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508456(A;A)
Make rs397508456(A;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117606673
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508456
ebirs397508456
HLIrs397508456
Exacrs397508456
Varsomers397508456
Maprs397508456
PheGenIrs397508456
hapmaprs397508456
1000 genomesrs397508456
hgdprs397508456
ensemblrs397508456
gopubmedrs397508456
geneviewrs397508456
scholarrs397508456
googlers397508456
pharmgkbrs397508456
gwascentralrs397508456
openSNPrs397508456
23andMers397508456
23andMe allrs397508456
SNP Nexus

SNPshotrs397508456
SNPdbers397508456
MSV3drs397508456
GWAS Ctlgrs397508456
Max Magnitude0
ClinVar
Risk rs397508456(A;A)
Alt rs397508456(A;A)
Reference rs397508456(G;G)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117246727G>A
CLNSRC ClinVar
CLNACC RCV000046716.2,