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rs397508573

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397508573(C;T)
Make rs397508573(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117627529
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508573
ebirs397508573
HLIrs397508573
Exacrs397508573
Varsomers397508573
Maprs397508573
PheGenIrs397508573
hapmaprs397508573
1000 genomesrs397508573
hgdprs397508573
ensemblrs397508573
gopubmedrs397508573
geneviewrs397508573
scholarrs397508573
googlers397508573
pharmgkbrs397508573
gwascentralrs397508573
openSNPrs397508573
23andMers397508573
23andMe allrs397508573
SNP Nexus

SNPshotrs397508573
SNPdbers397508573
MSV3drs397508573
GWAS Ctlgrs397508573
Max Magnitude0
ClinVar
Risk rs397508573(T;T)
Alt rs397508573(T;T)
Reference rs397508573(C;C)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117267583C>T
CLNSRC ClinVar
CLNACC RCV000046908.2,