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rs397508815

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397508815(C;T)
Make rs397508815(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117504287
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508815
ebirs397508815
HLIrs397508815
Exacrs397508815
Varsomers397508815
Maprs397508815
PheGenIrs397508815
hapmaprs397508815
1000 genomesrs397508815
hgdprs397508815
ensemblrs397508815
gopubmedrs397508815
geneviewrs397508815
scholarrs397508815
googlers397508815
pharmgkbrs397508815
gwascentralrs397508815
openSNPrs397508815
23andMers397508815
23andMe allrs397508815
SNP Nexus

SNPshotrs397508815
SNPdbers397508815
MSV3drs397508815
GWAS Ctlgrs397508815
Max Magnitude0
ClinVar
Risk rs397508815(T;T)
Alt rs397508815(T;T)
Reference rs397508815(C;C)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117144341C>T
CLNSRC ClinVar
CLNACC RCV000047281.2,