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rs397508556

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397508556(A;G)
Make rs397508556(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117614660
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508556
ebirs397508556
HLIrs397508556
Exacrs397508556
Varsomers397508556
Maprs397508556
PheGenIrs397508556
hapmaprs397508556
1000 genomesrs397508556
hgdprs397508556
ensemblrs397508556
gopubmedrs397508556
geneviewrs397508556
scholarrs397508556
googlers397508556
pharmgkbrs397508556
gwascentralrs397508556
openSNPrs397508556
23andMers397508556
23andMe allrs397508556
SNP Nexus

SNPshotrs397508556
SNPdbers397508556
MSV3drs397508556
GWAS Ctlgrs397508556
Max Magnitude0
ClinVar
Risk rs397508556(G;G)
Alt rs397508556(G;G)
Reference rs397508556(A;A)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117254714A>G
CLNSRC ClinVar
CLNACC RCV000046884.2,