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rs397508553

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397508553(A;G)
Make rs397508553(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117614654
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508553
ebirs397508553
HLIrs397508553
Exacrs397508553
Varsomers397508553
Maprs397508553
PheGenIrs397508553
hapmaprs397508553
1000 genomesrs397508553
hgdprs397508553
ensemblrs397508553
gopubmedrs397508553
geneviewrs397508553
scholarrs397508553
googlers397508553
pharmgkbrs397508553
gwascentralrs397508553
openSNPrs397508553
23andMers397508553
23andMe allrs397508553
SNP Nexus

SNPshotrs397508553
SNPdbers397508553
MSV3drs397508553
GWAS Ctlgrs397508553
Max Magnitude0
ClinVar
Risk rs397508553(G;G)
Alt rs397508553(G;G)
Reference rs397508553(A;A)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117254708A>G
CLNSRC ClinVar
CLNACC RCV000046881.2,