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

rs397508555

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397508555(G;G)
Make rs397508555(G;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117614655
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508555
ebirs397508555
HLIrs397508555
Exacrs397508555
Varsomers397508555
Maprs397508555
PheGenIrs397508555
hapmaprs397508555
1000 genomesrs397508555
hgdprs397508555
ensemblrs397508555
gopubmedrs397508555
geneviewrs397508555
scholarrs397508555
googlers397508555
pharmgkbrs397508555
gwascentralrs397508555
openSNPrs397508555
23andMers397508555
23andMe allrs397508555
SNP Nexus

SNPshotrs397508555
SNPdbers397508555
MSV3drs397508555
GWAS Ctlgrs397508555
Max Magnitude0
ClinVar
Risk rs397508555(C,G;C,G)
Alt rs397508555(C,G;C,G)
Reference rs397508555(T;T)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117254709T>G
CLNSRC ClinVar
CLNACC RCV000046883.2,