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rs397508663

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397508663(-;-)
Make rs397508663(-;A)
Make rs397508663(A;A)
ReferenceGRCh38 38.1/141
Chromosome7
Position117664763
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508663
ebirs397508663
HLIrs397508663
Exacrs397508663
Varsomers397508663
Maprs397508663
PheGenIrs397508663
hapmaprs397508663
1000 genomesrs397508663
hgdprs397508663
ensemblrs397508663
gopubmedrs397508663
geneviewrs397508663
scholarrs397508663
googlers397508663
pharmgkbrs397508663
gwascentralrs397508663
openSNPrs397508663
23andMers397508663
23andMe allrs397508663
SNP Nexus

SNPshotrs397508663
SNPdbers397508663
MSV3drs397508663
GWAS Ctlgrs397508663
Max Magnitude0
ClinVar
Risk rs397508663(A;A)
Alt rs397508663(A;A)
Reference rs397508663(;)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117304817dupA
CLNSRC ClinVar
CLNACC RCV000047060.2,