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rs397508319

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397508319(C;T)
Make rs397508319(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117592067
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508319
ebirs397508319
HLIrs397508319
Exacrs397508319
Varsomers397508319
Maprs397508319
PheGenIrs397508319
hapmaprs397508319
1000 genomesrs397508319
hgdprs397508319
ensemblrs397508319
gopubmedrs397508319
geneviewrs397508319
scholarrs397508319
googlers397508319
pharmgkbrs397508319
gwascentralrs397508319
openSNPrs397508319
23andMers397508319
23andMe allrs397508319
SNP Nexus

SNPshotrs397508319
SNPdbers397508319
MSV3drs397508319
GWAS Ctlgrs397508319
Max Magnitude0
ClinVar
Risk rs397508319(T;T)
Alt rs397508319(T;T)
Reference rs397508319(C;C)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117232121C>T
CLNSRC ClinVar
CLNACC RCV000046503.2,