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rs397508386

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397508386(A;G)
Make rs397508386(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117594928
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508386
ebirs397508386
HLIrs397508386
Exacrs397508386
Varsomers397508386
Maprs397508386
PheGenIrs397508386
hapmaprs397508386
1000 genomesrs397508386
hgdprs397508386
ensemblrs397508386
gopubmedrs397508386
geneviewrs397508386
scholarrs397508386
googlers397508386
pharmgkbrs397508386
gwascentralrs397508386
openSNPrs397508386
23andMers397508386
23andMe allrs397508386
SNP Nexus

SNPshotrs397508386
SNPdbers397508386
MSV3drs397508386
GWAS Ctlgrs397508386
Max Magnitude0
ClinVar
Risk rs397508386(G;G)
Alt rs397508386(G;G)
Reference rs397508386(A;A)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117234982A>G
CLNSRC ClinVar
CLNACC RCV000046605.2,