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rs397508581

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397508581(C;G)
Make rs397508581(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117627599
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508581
ebirs397508581
HLIrs397508581
Exacrs397508581
Varsomers397508581
Maprs397508581
PheGenIrs397508581
hapmaprs397508581
1000 genomesrs397508581
hgdprs397508581
ensemblrs397508581
gopubmedrs397508581
geneviewrs397508581
scholarrs397508581
googlers397508581
pharmgkbrs397508581
gwascentralrs397508581
openSNPrs397508581
23andMers397508581
23andMe allrs397508581
SNP Nexus

SNPshotrs397508581
SNPdbers397508581
MSV3drs397508581
GWAS Ctlgrs397508581
Max Magnitude0
ClinVar
Risk rs397508581(G;G)
Alt rs397508581(G;G)
Reference rs397508581(C;C)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117267653C>G
CLNSRC ClinVar
CLNACC RCV000046925.2,