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rs397508327

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508327(G;T)
Make rs397508327(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117592157
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508327
ebirs397508327
HLIrs397508327
Exacrs397508327
Varsomers397508327
Maprs397508327
PheGenIrs397508327
hapmaprs397508327
1000 genomesrs397508327
hgdprs397508327
ensemblrs397508327
gopubmedrs397508327
geneviewrs397508327
scholarrs397508327
googlers397508327
pharmgkbrs397508327
gwascentralrs397508327
openSNPrs397508327
23andMers397508327
23andMe allrs397508327
SNP Nexus

SNPshotrs397508327
SNPdbers397508327
MSV3drs397508327
GWAS Ctlgrs397508327
Max Magnitude0
ClinVar
Risk rs397508327(T;T)
Alt rs397508327(T;T)
Reference rs397508327(G;G)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117232211G>T
CLNSRC ClinVar
CLNACC RCV000046516.2,