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

rs397508318

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397508318(C;C)
Make rs397508318(C;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117592065
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508318
ebirs397508318
HLIrs397508318
Exacrs397508318
Varsomers397508318
Maprs397508318
PheGenIrs397508318
hapmaprs397508318
1000 genomesrs397508318
hgdprs397508318
ensemblrs397508318
gopubmedrs397508318
geneviewrs397508318
scholarrs397508318
googlers397508318
pharmgkbrs397508318
gwascentralrs397508318
openSNPrs397508318
23andMers397508318
23andMe allrs397508318
SNP Nexus

SNPshotrs397508318
SNPdbers397508318
MSV3drs397508318
GWAS Ctlgrs397508318
Max Magnitude0
ClinVar
Risk rs397508318(C;C)
Alt rs397508318(C;C)
Reference rs397508318(T;T)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117232119T>C
CLNSRC ClinVar
CLNACC RCV000046502.2,