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

rs397508371

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508371(A;A)
Make rs397508371(A;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117509105
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508371
ebirs397508371
HLIrs397508371
Exacrs397508371
Varsomers397508371
Maprs397508371
PheGenIrs397508371
hapmaprs397508371
1000 genomesrs397508371
hgdprs397508371
ensemblrs397508371
gopubmedrs397508371
geneviewrs397508371
scholarrs397508371
googlers397508371
pharmgkbrs397508371
gwascentralrs397508371
openSNPrs397508371
23andMers397508371
23andMe allrs397508371
SNP Nexus

SNPshotrs397508371
SNPdbers397508371
MSV3drs397508371
GWAS Ctlgrs397508371
Max Magnitude0
ClinVar
Risk rs397508371(A;A)
Alt rs397508371(A;A)
Reference rs397508371(G;G)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117149159G>A
CLNSRC ClinVar
CLNACC RCV000046584.2,