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rs397508266

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397508266(A;G)
Make rs397508266(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117589467
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508266
ebirs397508266
HLIrs397508266
Exacrs397508266
Varsomers397508266
Maprs397508266
PheGenIrs397508266
hapmaprs397508266
1000 genomesrs397508266
hgdprs397508266
ensemblrs397508266
gopubmedrs397508266
geneviewrs397508266
scholarrs397508266
googlers397508266
pharmgkbrs397508266
gwascentralrs397508266
openSNPrs397508266
23andMers397508266
23andMe allrs397508266
SNP Nexus

SNPshotrs397508266
SNPdbers397508266
MSV3drs397508266
GWAS Ctlgrs397508266
Max Magnitude0
ClinVar
Risk rs397508266(G;G)
Alt rs397508266(G;G)
Reference rs397508266(A;A)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117229521A>G
CLNSRC ClinVar
CLNACC RCV000046417.2,