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rs397508579

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397508579(-;-)
Make rs397508579(-;A)
ReferenceGRCh38 38.1/141
Chromosome7
Position117627583
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508579
ebirs397508579
HLIrs397508579
Exacrs397508579
Varsomers397508579
Maprs397508579
PheGenIrs397508579
hapmaprs397508579
1000 genomesrs397508579
hgdprs397508579
ensemblrs397508579
gopubmedrs397508579
geneviewrs397508579
scholarrs397508579
googlers397508579
pharmgkbrs397508579
gwascentralrs397508579
openSNPrs397508579
23andMers397508579
23andMe allrs397508579
SNP Nexus

SNPshotrs397508579
SNPdbers397508579
MSV3drs397508579
GWAS Ctlgrs397508579
Max Magnitude0
ClinVar
Risk rs397508579(;)
Alt rs397508579(;)
Reference rs397508579(A;A)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117267637delA
CLNSRC ClinVar
CLNACC RCV000046922.2,