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rs397508544

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397508544(C;C)
Make rs397508544(C;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117611810
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508544
ebirs397508544
HLIrs397508544
Exacrs397508544
Varsomers397508544
Maprs397508544
PheGenIrs397508544
hapmaprs397508544
1000 genomesrs397508544
hgdprs397508544
ensemblrs397508544
gopubmedrs397508544
geneviewrs397508544
scholarrs397508544
googlers397508544
pharmgkbrs397508544
gwascentralrs397508544
openSNPrs397508544
23andMers397508544
23andMe allrs397508544
SNP Nexus

SNPshotrs397508544
SNPdbers397508544
MSV3drs397508544
GWAS Ctlgrs397508544
Max Magnitude0
ClinVar
Risk rs397508544(C;C)
Alt rs397508544(C;C)
Reference rs397508544(T;T)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117251864T>C
CLNSRC ClinVar
CLNACC RCV000046872.2,