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rs397508358

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CC;CC) 0 common in clinvar
Make rs397508358(-;-)
Make rs397508358(-;CC)
ReferenceGRCh38 38.1/141
Chromosome7
Position117592443
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508358
ebirs397508358
HLIrs397508358
Exacrs397508358
Varsomers397508358
Maprs397508358
PheGenIrs397508358
hapmaprs397508358
1000 genomesrs397508358
hgdprs397508358
ensemblrs397508358
gopubmedrs397508358
geneviewrs397508358
scholarrs397508358
googlers397508358
pharmgkbrs397508358
gwascentralrs397508358
openSNPrs397508358
23andMers397508358
23andMe allrs397508358
SNP Nexus

SNPshotrs397508358
SNPdbers397508358
MSV3drs397508358
GWAS Ctlgrs397508358
Max Magnitude0
ClinVar
Risk rs397508358(;)
Alt rs397508358(;)
Reference rs397508358(CC;CC)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117232497_117232498delCC
CLNSRC ClinVar
CLNACC RCV000046567.2,