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rs397508181

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508181(-;-)
Make rs397508181(-;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117548665
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508181
ebirs397508181
HLIrs397508181
Exacrs397508181
Varsomers397508181
Maprs397508181
PheGenIrs397508181
hapmaprs397508181
1000 genomesrs397508181
hgdprs397508181
ensemblrs397508181
gopubmedrs397508181
geneviewrs397508181
scholarrs397508181
googlers397508181
pharmgkbrs397508181
gwascentralrs397508181
openSNPrs397508181
23andMers397508181
23andMe allrs397508181
SNP Nexus

SNPshotrs397508181
SNPdbers397508181
MSV3drs397508181
GWAS Ctlgrs397508181
Max Magnitude0
ClinVar
Risk rs397508181(;)
Alt rs397508181(;)
Reference rs397508181(G;G)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117188719delG
CLNSRC ClinVar
CLNACC RCV000046264.2,