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rs397508620

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397508620(C;T)
Make rs397508620(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117642591
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508620
ebirs397508620
HLIrs397508620
Exacrs397508620
Varsomers397508620
Maprs397508620
PheGenIrs397508620
hapmaprs397508620
1000 genomesrs397508620
hgdprs397508620
ensemblrs397508620
gopubmedrs397508620
geneviewrs397508620
scholarrs397508620
googlers397508620
pharmgkbrs397508620
gwascentralrs397508620
openSNPrs397508620
23andMers397508620
23andMe allrs397508620
SNP Nexus

SNPshotrs397508620
SNPdbers397508620
MSV3drs397508620
GWAS Ctlgrs397508620
Max Magnitude0
ClinVar
Risk rs397508620(T;T)
Alt rs397508620(T;T)
Reference rs397508620(C;C)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117282645C>T
CLNSRC ClinVar
CLNACC RCV000047001.2,