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rs397508441

From SNPedia

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


Make rs397508441(-;-)
ReferenceGRCh38 38.1/141
Chromosome7
Position117603699
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508441
ebirs397508441
HLIrs397508441
Exacrs397508441
Varsomers397508441
Maprs397508441
PheGenIrs397508441
hapmaprs397508441
1000 genomesrs397508441
hgdprs397508441
ensemblrs397508441
gopubmedrs397508441
geneviewrs397508441
scholarrs397508441
googlers397508441
pharmgkbrs397508441
gwascentralrs397508441
openSNPrs397508441
23andMers397508441
23andMe allrs397508441
SNP Nexus

SNPshotrs397508441
SNPdbers397508441
MSV3drs397508441
GWAS Ctlgrs397508441
Max Magnitude3
ClinVar
Risk rs397508441(;)
Alt rs397508441(;)
Reference rs397508441(T;T)
Significance Pathogenic
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117243753delT
CLNSRC CFTR2
CLNACC RCV000046696.3,