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rs397508316

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508316(A;A)
Make rs397508316(A;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117592049
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508316
ebirs397508316
HLIrs397508316
Exacrs397508316
Varsomers397508316
Maprs397508316
PheGenIrs397508316
hapmaprs397508316
1000 genomesrs397508316
hgdprs397508316
ensemblrs397508316
gopubmedrs397508316
geneviewrs397508316
scholarrs397508316
googlers397508316
pharmgkbrs397508316
gwascentralrs397508316
openSNPrs397508316
23andMers397508316
23andMe allrs397508316
SNP Nexus

SNPshotrs397508316
SNPdbers397508316
MSV3drs397508316
GWAS Ctlgrs397508316
Max Magnitude0
ClinVar
Risk rs397508316(A,C;A,C)
Alt rs397508316(A,C;A,C)
Reference rs397508316(G;G)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117232103G>A; NC_000007.13:g.117232103G>C
CLNSRC ClinVar
CLNACC RCV000046499.2, RCV000046500.2,