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

rs397508520

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397508520(C;T)
Make rs397508520(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117530948
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508520
ebirs397508520
HLIrs397508520
Exacrs397508520
Varsomers397508520
Maprs397508520
PheGenIrs397508520
hapmaprs397508520
1000 genomesrs397508520
hgdprs397508520
ensemblrs397508520
gopubmedrs397508520
geneviewrs397508520
scholarrs397508520
googlers397508520
pharmgkbrs397508520
gwascentralrs397508520
openSNPrs397508520
23andMers397508520
23andMe allrs397508520
SNP Nexus

SNPshotrs397508520
SNPdbers397508520
MSV3drs397508520
GWAS Ctlgrs397508520
Max Magnitude0
ClinVar
Risk rs397508520(T;T)
Alt rs397508520(T;T)
Reference rs397508520(C;C)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117171002C>T
CLNSRC ClinVar
CLNACC RCV000046833.2,