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rs397508580

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397508580(-;-)
Make rs397508580(-;A)
ReferenceGRCh38 38.1/141
Chromosome7
Position117627593
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508580
ebirs397508580
HLIrs397508580
Exacrs397508580
Varsomers397508580
Maprs397508580
PheGenIrs397508580
hapmaprs397508580
1000 genomesrs397508580
hgdprs397508580
ensemblrs397508580
gopubmedrs397508580
geneviewrs397508580
scholarrs397508580
googlers397508580
pharmgkbrs397508580
gwascentralrs397508580
openSNPrs397508580
23andMers397508580
23andMe allrs397508580
SNP Nexus

SNPshotrs397508580
SNPdbers397508580
MSV3drs397508580
GWAS Ctlgrs397508580
Max Magnitude0
ClinVar
Risk rs397508580(;)
Alt rs397508580(;)
Reference rs397508580(A;A)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117267647delA
CLNSRC ClinVar
CLNACC RCV000046924.2,