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rs397508730

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397508730(A;C)
Make rs397508730(C;C)
ReferenceGRCh38 38.1/141
Chromosome7
Position117531107
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508730
ebirs397508730
HLIrs397508730
Exacrs397508730
Varsomers397508730
Maprs397508730
PheGenIrs397508730
hapmaprs397508730
1000 genomesrs397508730
hgdprs397508730
ensemblrs397508730
gopubmedrs397508730
geneviewrs397508730
scholarrs397508730
googlers397508730
pharmgkbrs397508730
gwascentralrs397508730
openSNPrs397508730
23andMers397508730
23andMe allrs397508730
SNP Nexus

SNPshotrs397508730
SNPdbers397508730
MSV3drs397508730
GWAS Ctlgrs397508730
Max Magnitude0
ClinVar
Risk rs397508730(C,G;C,G)
Alt rs397508730(C,G;C,G)
Reference rs397508730(A;A)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117171161A>C; NC_000007.13:g.117171161A>G
CLNSRC ClinVar
CLNACC RCV000047156.2, RCV000047157.2,