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rs397508348

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397508348(-;-)
Make rs397508348(-;C)
ReferenceGRCh38 38.1/141
Chromosome7
Position117509086
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508348
ebirs397508348
HLIrs397508348
Exacrs397508348
Varsomers397508348
Maprs397508348
PheGenIrs397508348
hapmaprs397508348
1000 genomesrs397508348
hgdprs397508348
ensemblrs397508348
gopubmedrs397508348
geneviewrs397508348
scholarrs397508348
googlers397508348
pharmgkbrs397508348
gwascentralrs397508348
openSNPrs397508348
23andMers397508348
23andMe allrs397508348
SNP Nexus

SNPshotrs397508348
SNPdbers397508348
MSV3drs397508348
GWAS Ctlgrs397508348
Max Magnitude0
ClinVar
Risk rs397508348(;)
Alt rs397508348(;)
Reference rs397508348(C;C)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117149140delC
CLNSRC ClinVar
CLNACC RCV000046549.2,