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rs397508151

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508151(-;-)
Make rs397508151(-;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117540299
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508151
ebirs397508151
HLIrs397508151
Exacrs397508151
Varsomers397508151
Maprs397508151
PheGenIrs397508151
hapmaprs397508151
1000 genomesrs397508151
hgdprs397508151
ensemblrs397508151
gopubmedrs397508151
geneviewrs397508151
scholarrs397508151
googlers397508151
pharmgkbrs397508151
gwascentralrs397508151
openSNPrs397508151
23andMers397508151
23andMe allrs397508151
SNP Nexus

SNPshotrs397508151
SNPdbers397508151
MSV3drs397508151
GWAS Ctlgrs397508151
Max Magnitude0
ClinVar
Risk rs397508151(;)
Alt rs397508151(;)
Reference rs397508151(G;G)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117180353delG
CLNSRC ClinVar
CLNACC RCV000046219.2,