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rs397508680

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397508680(-;-)
Make rs397508680(-;C)
ReferenceGRCh38 38.1/141
Chromosome7
Position117665461
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508680
ebirs397508680
HLIrs397508680
Exacrs397508680
Varsomers397508680
Maprs397508680
PheGenIrs397508680
hapmaprs397508680
1000 genomesrs397508680
hgdprs397508680
ensemblrs397508680
gopubmedrs397508680
geneviewrs397508680
scholarrs397508680
googlers397508680
pharmgkbrs397508680
gwascentralrs397508680
openSNPrs397508680
23andMers397508680
23andMe allrs397508680
SNP Nexus

SNPshotrs397508680
SNPdbers397508680
MSV3drs397508680
GWAS Ctlgrs397508680
Max Magnitude0
ClinVar
Risk rs397508680(;)
Alt rs397508680(;)
Reference rs397508680(C;C)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117305515delC
CLNSRC ClinVar
CLNACC RCV000047083.2,