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rs397508337

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508337(G;T)
Make rs397508337(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117592241
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508337
ebirs397508337
HLIrs397508337
Exacrs397508337
Varsomers397508337
Maprs397508337
PheGenIrs397508337
hapmaprs397508337
1000 genomesrs397508337
hgdprs397508337
ensemblrs397508337
gopubmedrs397508337
geneviewrs397508337
scholarrs397508337
googlers397508337
pharmgkbrs397508337
gwascentralrs397508337
openSNPrs397508337
23andMers397508337
23andMe allrs397508337
SNP Nexus

SNPshotrs397508337
SNPdbers397508337
MSV3drs397508337
GWAS Ctlgrs397508337
Max Magnitude0
ClinVar
Risk rs397508337(T;T)
Alt rs397508337(T;T)
Reference rs397508337(G;G)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117232295G>T
CLNSRC ClinVar
CLNACC RCV000046533.2,