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rs397508223

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508223(C;C)
Make rs397508223(C;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117559581
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508223
ebirs397508223
HLIrs397508223
Exacrs397508223
Varsomers397508223
Maprs397508223
PheGenIrs397508223
hapmaprs397508223
1000 genomesrs397508223
hgdprs397508223
ensemblrs397508223
gopubmedrs397508223
geneviewrs397508223
scholarrs397508223
googlers397508223
pharmgkbrs397508223
gwascentralrs397508223
openSNPrs397508223
23andMers397508223
23andMe allrs397508223
SNP Nexus

SNPshotrs397508223
SNPdbers397508223
MSV3drs397508223
GWAS Ctlgrs397508223
Max Magnitude0
ClinVar
Risk rs397508223(C,T;C,T)
Alt rs397508223(C,T;C,T)
Reference rs397508223(G;G)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117199635G>C; NC_000007.13:g.117199635G>T
CLNSRC ClinVar
CLNACC RCV000046327.2, RCV000046328.2,