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rs397508485

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397508485(-;-)
Make rs397508485(-;C)
Make rs397508485(C;C)
ReferenceGRCh38 38.1/141
Chromosome7
Position117610569
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508485
ebirs397508485
HLIrs397508485
Exacrs397508485
Varsomers397508485
Maprs397508485
PheGenIrs397508485
hapmaprs397508485
1000 genomesrs397508485
hgdprs397508485
ensemblrs397508485
gopubmedrs397508485
geneviewrs397508485
scholarrs397508485
googlers397508485
pharmgkbrs397508485
gwascentralrs397508485
openSNPrs397508485
23andMers397508485
23andMe allrs397508485
SNP Nexus

SNPshotrs397508485
SNPdbers397508485
MSV3drs397508485
GWAS Ctlgrs397508485
Max Magnitude0
ClinVar
Risk rs397508485(C;C)
Alt rs397508485(C;C)
Reference rs397508485(;)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117250623dupC
CLNSRC ClinVar
CLNACC RCV000046764.2,