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rs397508645

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508645(A;A)
Make rs397508645(A;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117652897
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508645
ebirs397508645
HLIrs397508645
Exacrs397508645
Varsomers397508645
Maprs397508645
PheGenIrs397508645
hapmaprs397508645
1000 genomesrs397508645
hgdprs397508645
ensemblrs397508645
gopubmedrs397508645
geneviewrs397508645
scholarrs397508645
googlers397508645
pharmgkbrs397508645
gwascentralrs397508645
openSNPrs397508645
23andMers397508645
23andMe allrs397508645
SNP Nexus

SNPshotrs397508645
SNPdbers397508645
MSV3drs397508645
GWAS Ctlgrs397508645
Max Magnitude0
ClinVar
Risk rs397508645(A;A)
Alt rs397508645(A;A)
Reference rs397508645(G;G)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117292951G>A
CLNSRC ClinVar
CLNACC RCV000047036.2,