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rs397508571

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508571(A;A)
Make rs397508571(A;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117530971
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508571
ebirs397508571
HLIrs397508571
Exacrs397508571
Varsomers397508571
Maprs397508571
PheGenIrs397508571
hapmaprs397508571
1000 genomesrs397508571
hgdprs397508571
ensemblrs397508571
gopubmedrs397508571
geneviewrs397508571
scholarrs397508571
googlers397508571
pharmgkbrs397508571
gwascentralrs397508571
openSNPrs397508571
23andMers397508571
23andMe allrs397508571
SNP Nexus

SNPshotrs397508571
SNPdbers397508571
MSV3drs397508571
GWAS Ctlgrs397508571
Max Magnitude0
ClinVar
Risk rs397508571(A,C;A,C)
Alt rs397508571(A,C;A,C)
Reference rs397508571(G;G)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117171025G>A; NC_000007.13:g.117171025G>C
CLNSRC ClinVar
CLNACC RCV000046904.2, RCV000046905.2,