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rs397508171

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508171(-;-)
Make rs397508171(-;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117542076
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508171
ebirs397508171
HLIrs397508171
Exacrs397508171
Varsomers397508171
Maprs397508171
PheGenIrs397508171
hapmaprs397508171
1000 genomesrs397508171
hgdprs397508171
ensemblrs397508171
gopubmedrs397508171
geneviewrs397508171
scholarrs397508171
googlers397508171
pharmgkbrs397508171
gwascentralrs397508171
openSNPrs397508171
23andMers397508171
23andMe allrs397508171
SNP Nexus

SNPshotrs397508171
SNPdbers397508171
MSV3drs397508171
GWAS Ctlgrs397508171
Max Magnitude0
ClinVar
Risk rs397508171(;)
Alt rs397508171(;)
Reference rs397508171(G;G)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117182130delG
CLNSRC ClinVar
CLNACC RCV000046252.2,