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rs397508735

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397508735(A;G)
Make rs397508735(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117534274
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508735
ebirs397508735
HLIrs397508735
Exacrs397508735
Varsomers397508735
Maprs397508735
PheGenIrs397508735
hapmaprs397508735
1000 genomesrs397508735
hgdprs397508735
ensemblrs397508735
gopubmedrs397508735
geneviewrs397508735
scholarrs397508735
googlers397508735
pharmgkbrs397508735
gwascentralrs397508735
openSNPrs397508735
23andMers397508735
23andMe allrs397508735
SNP Nexus

SNPshotrs397508735
SNPdbers397508735
MSV3drs397508735
GWAS Ctlgrs397508735
Max Magnitude0
ClinVar
Risk rs397508735(G;G)
Alt rs397508735(G;G)
Reference rs397508735(A;A)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117174328A>G
CLNSRC ClinVar
CLNACC RCV000047166.2,