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rs397508816

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397508816(C;G)
Make rs397508816(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117540142
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508816
ebirs397508816
HLIrs397508816
Exacrs397508816
Varsomers397508816
Maprs397508816
PheGenIrs397508816
hapmaprs397508816
1000 genomesrs397508816
hgdprs397508816
ensemblrs397508816
gopubmedrs397508816
geneviewrs397508816
scholarrs397508816
googlers397508816
pharmgkbrs397508816
gwascentralrs397508816
openSNPrs397508816
23andMers397508816
23andMe allrs397508816
SNP Nexus

SNPshotrs397508816
SNPdbers397508816
MSV3drs397508816
GWAS Ctlgrs397508816
Max Magnitude0
ClinVar
Risk rs397508816(G,T;G,T)
Alt rs397508816(G,T;G,T)
Reference rs397508816(C;C)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117180196C>G
CLNSRC ClinVar
CLNACC RCV000047283.2,