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rs397508257

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397508257(-;-)
Make rs397508257(-;C)
ReferenceGRCh38 38.1/141
Chromosome7
Position117587824
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508257
ebirs397508257
HLIrs397508257
Exacrs397508257
Varsomers397508257
Maprs397508257
PheGenIrs397508257
hapmaprs397508257
1000 genomesrs397508257
hgdprs397508257
ensemblrs397508257
gopubmedrs397508257
geneviewrs397508257
scholarrs397508257
googlers397508257
pharmgkbrs397508257
gwascentralrs397508257
openSNPrs397508257
23andMers397508257
23andMe allrs397508257
SNP Nexus

SNPshotrs397508257
SNPdbers397508257
MSV3drs397508257
GWAS Ctlgrs397508257
Max Magnitude0
ClinVar
Risk rs397508257(;)
Alt rs397508257(;)
Reference rs397508257(C;C)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117227878delC
CLNSRC ClinVar
CLNACC RCV000046400.2,