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rs397508267

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
(A;G) 3 carrier of a cystic fibrosis allele
Make rs397508267(A;C)
Make rs397508267(C;C)
ReferenceGRCh38 38.1/141
Chromosome7
Position117590353
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508267
ebirs397508267
HLIrs397508267
Exacrs397508267
Varsomers397508267
Maprs397508267
PheGenIrs397508267
hapmaprs397508267
1000 genomesrs397508267
hgdprs397508267
ensemblrs397508267
gopubmedrs397508267
geneviewrs397508267
scholarrs397508267
googlers397508267
pharmgkbrs397508267
gwascentralrs397508267
openSNPrs397508267
23andMers397508267
23andMe allrs397508267
SNP Nexus

SNPshotrs397508267
SNPdbers397508267
MSV3drs397508267
GWAS Ctlgrs397508267
Max Magnitude3
ClinVar
Risk rs397508267(C;C)
Alt rs397508267(C;C)
Reference rs397508267(A;A)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117230407A>C
CLNSRC ClinVar
CLNACC RCV000046418.2,