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rs397508560

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397508560(C;T)
Make rs397508560(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117614675
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508560
ebirs397508560
HLIrs397508560
Exacrs397508560
Varsomers397508560
Maprs397508560
PheGenIrs397508560
hapmaprs397508560
1000 genomesrs397508560
hgdprs397508560
ensemblrs397508560
gopubmedrs397508560
geneviewrs397508560
scholarrs397508560
googlers397508560
pharmgkbrs397508560
gwascentralrs397508560
openSNPrs397508560
23andMers397508560
23andMe allrs397508560
SNP Nexus

SNPshotrs397508560
SNPdbers397508560
MSV3drs397508560
GWAS Ctlgrs397508560
Max Magnitude0
ClinVar
Risk rs397508560(T;T)
Alt rs397508560(T;T)
Reference rs397508560(C;C)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117254729C>T
CLNSRC ClinVar
CLNACC RCV000046888.2,