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rs397508787

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397508787(-;-)
Make rs397508787(-;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117535382
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508787
ebirs397508787
HLIrs397508787
Exacrs397508787
Varsomers397508787
Maprs397508787
PheGenIrs397508787
hapmaprs397508787
1000 genomesrs397508787
hgdprs397508787
ensemblrs397508787
gopubmedrs397508787
geneviewrs397508787
scholarrs397508787
googlers397508787
pharmgkbrs397508787
gwascentralrs397508787
openSNPrs397508787
23andMers397508787
23andMe allrs397508787
SNP Nexus

SNPshotrs397508787
SNPdbers397508787
MSV3drs397508787
GWAS Ctlgrs397508787
Max Magnitude0
ClinVar
Risk rs397508787(;)
Alt rs397508787(;)
Reference rs397508787(T;T)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117175436delT
CLNSRC ClinVar
CLNACC RCV000047239.2,