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

rs397508364

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AC;AC) 0 common in clinvar
Make rs397508364(-;-)
Make rs397508364(-;AC)
ReferenceGRCh38 38.1/141
Chromosome7
Position117592491
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508364
ebirs397508364
HLIrs397508364
Exacrs397508364
Varsomers397508364
Maprs397508364
PheGenIrs397508364
hapmaprs397508364
1000 genomesrs397508364
hgdprs397508364
ensemblrs397508364
gopubmedrs397508364
geneviewrs397508364
scholarrs397508364
googlers397508364
pharmgkbrs397508364
gwascentralrs397508364
openSNPrs397508364
23andMers397508364
23andMe allrs397508364
SNP Nexus

SNPshotrs397508364
SNPdbers397508364
MSV3drs397508364
GWAS Ctlgrs397508364
Max Magnitude0
ClinVar
Risk rs397508364(;)
Alt rs397508364(;)
Reference rs397508364(AC;AC)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117232545_117232546delAC
CLNSRC ClinVar
CLNACC RCV000046575.2,