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rs397508540

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508540(-;-)
Make rs397508540(-;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117611756
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508540
ClinGenrs397508540
ebirs397508540
HLIrs397508540
Exacrs397508540
Varsomers397508540
Maprs397508540
PheGenIrs397508540
hapmaprs397508540
1000 genomesrs397508540
hgdprs397508540
ensemblrs397508540
gopubmedrs397508540
geneviewrs397508540
scholarrs397508540
googlers397508540
pharmgkbrs397508540
gwascentralrs397508540
openSNPrs397508540
23andMers397508540
23andMe allrs397508540
SNP Nexus

SNPshotrs397508540
SNPdbers397508540
MSV3drs397508540
GWAS Ctlgrs397508540
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs397508540(G;G)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117251810delG
CLNSRC ClinVar
CLNACC RCV000046865.2,