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rs397508762

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508762(G;T)
Make rs397508762(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117504256
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508762
ebirs397508762
HLIrs397508762
Exacrs397508762
Varsomers397508762
Maprs397508762
PheGenIrs397508762
hapmaprs397508762
1000 genomesrs397508762
hgdprs397508762
ensemblrs397508762
gopubmedrs397508762
geneviewrs397508762
scholarrs397508762
googlers397508762
pharmgkbrs397508762
gwascentralrs397508762
openSNPrs397508762
23andMers397508762
23andMe allrs397508762
SNP Nexus

SNPshotrs397508762
SNPdbers397508762
MSV3drs397508762
GWAS Ctlgrs397508762
Max Magnitude0
ClinVar
Risk rs397508762(T;T)
Alt rs397508762(T;T)
Reference rs397508762(G;G)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117144310G>T
CLNSRC ClinVar
CLNACC RCV000047206.2,