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rs397508216

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508216(A;A)
Make rs397508216(A;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117559558
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508216
ebirs397508216
HLIrs397508216
Exacrs397508216
Varsomers397508216
Maprs397508216
PheGenIrs397508216
hapmaprs397508216
1000 genomesrs397508216
hgdprs397508216
ensemblrs397508216
gopubmedrs397508216
geneviewrs397508216
scholarrs397508216
googlers397508216
pharmgkbrs397508216
gwascentralrs397508216
openSNPrs397508216
23andMers397508216
23andMe allrs397508216
SNP Nexus

SNPshotrs397508216
SNPdbers397508216
MSV3drs397508216
GWAS Ctlgrs397508216
Max Magnitude0
ClinVar
Risk rs397508216(A;A)
Alt rs397508216(A;A)
Reference rs397508216(G;G)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117199612G>A
CLNSRC ClinVar
CLNACC RCV000046318.2,