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rs397508323

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508323(G;T)
Make rs397508323(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117592133
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508323
ebirs397508323
HLIrs397508323
Exacrs397508323
Varsomers397508323
Maprs397508323
PheGenIrs397508323
hapmaprs397508323
1000 genomesrs397508323
hgdprs397508323
ensemblrs397508323
gopubmedrs397508323
geneviewrs397508323
scholarrs397508323
googlers397508323
pharmgkbrs397508323
gwascentralrs397508323
openSNPrs397508323
23andMers397508323
23andMe allrs397508323
SNP Nexus

SNPshotrs397508323
SNPdbers397508323
MSV3drs397508323
GWAS Ctlgrs397508323
Max Magnitude0
ClinVar
Risk rs397508323(T;T)
Alt rs397508323(T;T)
Reference rs397508323(G;G)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117232187G>T
CLNSRC ClinVar
CLNACC RCV000046510.2,