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rs397508373

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397508373(C;G)
Make rs397508373(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117592566
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508373
ebirs397508373
HLIrs397508373
Exacrs397508373
Varsomers397508373
Maprs397508373
PheGenIrs397508373
hapmaprs397508373
1000 genomesrs397508373
hgdprs397508373
ensemblrs397508373
gopubmedrs397508373
geneviewrs397508373
scholarrs397508373
googlers397508373
pharmgkbrs397508373
gwascentralrs397508373
openSNPrs397508373
23andMers397508373
23andMe allrs397508373
SNP Nexus

SNPshotrs397508373
SNPdbers397508373
MSV3drs397508373
GWAS Ctlgrs397508373
Max Magnitude0
ClinVar
Risk rs397508373(G;G)
Alt rs397508373(G;G)
Reference rs397508373(C;C)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117232620C>G
CLNSRC ClinVar
CLNACC RCV000046588.2,