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

rs397508197

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508197(A;A)
Make rs397508197(A;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117548824
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508197
ebirs397508197
HLIrs397508197
Exacrs397508197
Varsomers397508197
Maprs397508197
PheGenIrs397508197
hapmaprs397508197
1000 genomesrs397508197
hgdprs397508197
ensemblrs397508197
gopubmedrs397508197
geneviewrs397508197
scholarrs397508197
googlers397508197
pharmgkbrs397508197
gwascentralrs397508197
openSNPrs397508197
23andMers397508197
23andMe allrs397508197
SNP Nexus

SNPshotrs397508197
SNPdbers397508197
MSV3drs397508197
GWAS Ctlgrs397508197
Max Magnitude0
ClinVar
Risk rs397508197(A;A)
Alt rs397508197(A;A)
Reference rs397508197(G;G)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117188878G>A
CLNSRC ClinVar
CLNACC RCV000046287.2,