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rs397508570

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397508570(A;G)
Make rs397508570(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117627520
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508570
ebirs397508570
HLIrs397508570
Exacrs397508570
Varsomers397508570
Maprs397508570
PheGenIrs397508570
hapmaprs397508570
1000 genomesrs397508570
hgdprs397508570
ensemblrs397508570
gopubmedrs397508570
geneviewrs397508570
scholarrs397508570
googlers397508570
pharmgkbrs397508570
gwascentralrs397508570
openSNPrs397508570
23andMers397508570
23andMe allrs397508570
SNP Nexus

SNPshotrs397508570
SNPdbers397508570
MSV3drs397508570
GWAS Ctlgrs397508570
Max Magnitude0
ClinVar
Risk rs397508570(G;G)
Alt rs397508570(G;G)
Reference rs397508570(A;A)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117267574A>G
CLNSRC ClinVar
CLNACC RCV000046902.2,