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rs397508608

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397508608(-;-)
Make rs397508608(-;G)
Make rs397508608(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117642494
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508608
ebirs397508608
HLIrs397508608
Exacrs397508608
Varsomers397508608
Maprs397508608
PheGenIrs397508608
hapmaprs397508608
1000 genomesrs397508608
hgdprs397508608
ensemblrs397508608
gopubmedrs397508608
geneviewrs397508608
scholarrs397508608
googlers397508608
pharmgkbrs397508608
gwascentralrs397508608
openSNPrs397508608
23andMers397508608
23andMe allrs397508608
SNP Nexus

SNPshotrs397508608
SNPdbers397508608
MSV3drs397508608
GWAS Ctlgrs397508608
Max Magnitude0
ClinVar
Risk rs397508608(G;G)
Alt rs397508608(G;G)
Reference rs397508608(;)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117282548dupG
CLNSRC ClinVar
CLNACC RCV000046982.2,