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rs397508503

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508503(A;A)
Make rs397508503(A;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117610670
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508503
ebirs397508503
HLIrs397508503
Exacrs397508503
Varsomers397508503
Maprs397508503
PheGenIrs397508503
hapmaprs397508503
1000 genomesrs397508503
hgdprs397508503
ensemblrs397508503
gopubmedrs397508503
geneviewrs397508503
scholarrs397508503
googlers397508503
pharmgkbrs397508503
gwascentralrs397508503
openSNPrs397508503
23andMers397508503
23andMe allrs397508503
SNP Nexus

SNPshotrs397508503
SNPdbers397508503
MSV3drs397508503
GWAS Ctlgrs397508503
Max Magnitude0
ClinVar
Risk rs397508503(A,T;A,T)
Alt rs397508503(A,T;A,T)
Reference rs397508503(G;G)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117250724G>A; NC_000007.13:g.117250724G>T
CLNSRC ClinVar
CLNACC RCV000046788.2, RCV000046789.2,