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rs397508585

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508585(-;-)
Make rs397508585(-;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117627645
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508585
ebirs397508585
HLIrs397508585
Exacrs397508585
Varsomers397508585
Maprs397508585
PheGenIrs397508585
hapmaprs397508585
1000 genomesrs397508585
hgdprs397508585
ensemblrs397508585
gopubmedrs397508585
geneviewrs397508585
scholarrs397508585
googlers397508585
pharmgkbrs397508585
gwascentralrs397508585
openSNPrs397508585
23andMers397508585
23andMe allrs397508585
SNP Nexus

SNPshotrs397508585
SNPdbers397508585
MSV3drs397508585
GWAS Ctlgrs397508585
Max Magnitude0
ClinVar
Risk rs397508585(;)
Alt rs397508585(;)
Reference rs397508585(G;G)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117267699delG
CLNSRC ClinVar
CLNACC RCV000046931.2,