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

rs397508478

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508478(G;T)
Make rs397508478(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117610537
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508478
ebirs397508478
HLIrs397508478
Exacrs397508478
Varsomers397508478
Maprs397508478
PheGenIrs397508478
hapmaprs397508478
1000 genomesrs397508478
hgdprs397508478
ensemblrs397508478
gopubmedrs397508478
geneviewrs397508478
scholarrs397508478
googlers397508478
pharmgkbrs397508478
gwascentralrs397508478
openSNPrs397508478
23andMers397508478
23andMe allrs397508478
SNP Nexus

SNPshotrs397508478
SNPdbers397508478
MSV3drs397508478
GWAS Ctlgrs397508478
Max Magnitude0
ClinVar
Risk rs397508478(T;T)
Alt rs397508478(T;T)
Reference rs397508478(G;G)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117250591G>T
CLNSRC ClinVar
CLNACC RCV000046753.2,