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rs397508704

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508704(C;C)
Make rs397508704(C;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117666907
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508704
ebirs397508704
HLIrs397508704
Exacrs397508704
Varsomers397508704
Maprs397508704
PheGenIrs397508704
hapmaprs397508704
1000 genomesrs397508704
hgdprs397508704
ensemblrs397508704
gopubmedrs397508704
geneviewrs397508704
scholarrs397508704
googlers397508704
pharmgkbrs397508704
gwascentralrs397508704
openSNPrs397508704
23andMers397508704
23andMe allrs397508704
SNP Nexus

SNPshotrs397508704
SNPdbers397508704
MSV3drs397508704
GWAS Ctlgrs397508704
Max Magnitude0
ClinVar
Risk rs397508704(C;C)
Alt rs397508704(C;C)
Reference rs397508704(G;G)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117306961G>C
CLNSRC ClinVar
CLNACC RCV000047116.2,