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rs397508672

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;C) 3 carrier of a cystic fibrosis allele
(C;C) 0 common in clinvar


Make rs397508672(-;-)
ReferenceGRCh38 38.1/141
Chromosome7
Position117531034
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508672
ebirs397508672
HLIrs397508672
Exacrs397508672
Varsomers397508672
Maprs397508672
PheGenIrs397508672
hapmaprs397508672
1000 genomesrs397508672
hgdprs397508672
ensemblrs397508672
gopubmedrs397508672
geneviewrs397508672
scholarrs397508672
googlers397508672
pharmgkbrs397508672
gwascentralrs397508672
openSNPrs397508672
23andMers397508672
23andMe allrs397508672
SNP Nexus

SNPshotrs397508672
SNPdbers397508672
MSV3drs397508672
GWAS Ctlgrs397508672
Max Magnitude3
ClinVar
Risk rs397508672(;)
Alt rs397508672(;)
Reference rs397508672(C;C)
Significance Pathogenic
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117171088delC
CLNSRC CFTR2
CLNACC RCV000047072.3,