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rs397508413

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508413(A;A)
Make rs397508413(A;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117602851
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508413
ebirs397508413
HLIrs397508413
Exacrs397508413
Varsomers397508413
Maprs397508413
PheGenIrs397508413
hapmaprs397508413
1000 genomesrs397508413
hgdprs397508413
ensemblrs397508413
gopubmedrs397508413
geneviewrs397508413
scholarrs397508413
googlers397508413
pharmgkbrs397508413
gwascentralrs397508413
openSNPrs397508413
23andMers397508413
23andMe allrs397508413
SNP Nexus

SNPshotrs397508413
SNPdbers397508413
MSV3drs397508413
GWAS Ctlgrs397508413
Max Magnitude0
ClinVar
Risk rs397508413(A;A)
Alt rs397508413(A;A)
Reference rs397508413(G;G)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117242905G>A
CLNSRC ClinVar
CLNACC RCV000046645.2,