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rs397508410

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508410(C;C)
Make rs397508410(C;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117602825
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508410
ebirs397508410
HLIrs397508410
Exacrs397508410
Varsomers397508410
Maprs397508410
PheGenIrs397508410
hapmaprs397508410
1000 genomesrs397508410
hgdprs397508410
ensemblrs397508410
gopubmedrs397508410
geneviewrs397508410
scholarrs397508410
googlers397508410
pharmgkbrs397508410
gwascentralrs397508410
openSNPrs397508410
23andMers397508410
23andMe allrs397508410
SNP Nexus

SNPshotrs397508410
SNPdbers397508410
MSV3drs397508410
GWAS Ctlgrs397508410
Max Magnitude0
ClinVar
Risk rs397508410(C,T;C,T)
Alt rs397508410(C,T;C,T)
Reference rs397508410(G;G)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117242879G>C; NC_000007.13:g.117242879G>T
CLNSRC ClinVar
CLNACC RCV000046636.2, RCV000046637.2,