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

rs397508426

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397508426(A;G)
Make rs397508426(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117530897
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508426
ebirs397508426
HLIrs397508426
Exacrs397508426
Varsomers397508426
Maprs397508426
PheGenIrs397508426
hapmaprs397508426
1000 genomesrs397508426
hgdprs397508426
ensemblrs397508426
gopubmedrs397508426
geneviewrs397508426
scholarrs397508426
googlers397508426
pharmgkbrs397508426
gwascentralrs397508426
openSNPrs397508426
23andMers397508426
23andMe allrs397508426
SNP Nexus

SNPshotrs397508426
SNPdbers397508426
MSV3drs397508426
GWAS Ctlgrs397508426
Max Magnitude0
ClinVar
Risk rs397508426(G;G)
Alt rs397508426(G;G)
Reference rs397508426(A;A)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117170951A>G
CLNSRC ClinVar
CLNACC RCV000046675.2,