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rs397508182

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397508182(-;-)
Make rs397508182(-;C)
ReferenceGRCh38 38.1/141
Chromosome7
Position117548666
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508182
ebirs397508182
HLIrs397508182
Exacrs397508182
Varsomers397508182
Maprs397508182
PheGenIrs397508182
hapmaprs397508182
1000 genomesrs397508182
hgdprs397508182
ensemblrs397508182
gopubmedrs397508182
geneviewrs397508182
scholarrs397508182
googlers397508182
pharmgkbrs397508182
gwascentralrs397508182
openSNPrs397508182
23andMers397508182
23andMe allrs397508182
SNP Nexus

SNPshotrs397508182
SNPdbers397508182
MSV3drs397508182
GWAS Ctlgrs397508182
Max Magnitude0
ClinVar
Risk rs397508182(;)
Alt rs397508182(;)
Reference rs397508182(C;C)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117188720delC
CLNSRC ClinVar
CLNACC RCV000046265.2,