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rs397508349

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508349(G;T)
Make rs397508349(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117592355
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508349
ebirs397508349
HLIrs397508349
Exacrs397508349
Varsomers397508349
Maprs397508349
PheGenIrs397508349
hapmaprs397508349
1000 genomesrs397508349
hgdprs397508349
ensemblrs397508349
gopubmedrs397508349
geneviewrs397508349
scholarrs397508349
googlers397508349
pharmgkbrs397508349
gwascentralrs397508349
openSNPrs397508349
23andMers397508349
23andMe allrs397508349
SNP Nexus

SNPshotrs397508349
SNPdbers397508349
MSV3drs397508349
GWAS Ctlgrs397508349
Max Magnitude0
ClinVar
Risk rs397508349(T;T)
Alt rs397508349(T;T)
Reference rs397508349(G;G)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117232409G>T
CLNSRC ClinVar
CLNACC RCV000046550.2,