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

rs397508388

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397508388(A;A)
Make rs397508388(A;C)
ReferenceGRCh38 38.1/141
Chromosome7
Position117594935
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508388
ebirs397508388
HLIrs397508388
Exacrs397508388
Varsomers397508388
Maprs397508388
PheGenIrs397508388
hapmaprs397508388
1000 genomesrs397508388
hgdprs397508388
ensemblrs397508388
gopubmedrs397508388
geneviewrs397508388
scholarrs397508388
googlers397508388
pharmgkbrs397508388
gwascentralrs397508388
openSNPrs397508388
23andMers397508388
23andMe allrs397508388
SNP Nexus

SNPshotrs397508388
SNPdbers397508388
MSV3drs397508388
GWAS Ctlgrs397508388
Max Magnitude0
ClinVar
Risk rs397508388(A;A)
Alt rs397508388(A;A)
Reference rs397508388(C;C)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117234989C>A
CLNSRC ClinVar
CLNACC RCV000046607.2,