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rs397508499

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;A) 3 carrier of a cystic fibrosis allele
(A;A) 0 common in clinvar


Make rs397508499(-;-)
ReferenceGRCh38 38.1/141
Chromosome7
Position117530935
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508499
ebirs397508499
HLIrs397508499
Exacrs397508499
Varsomers397508499
Maprs397508499
PheGenIrs397508499
hapmaprs397508499
1000 genomesrs397508499
hgdprs397508499
ensemblrs397508499
gopubmedrs397508499
geneviewrs397508499
scholarrs397508499
googlers397508499
pharmgkbrs397508499
gwascentralrs397508499
openSNPrs397508499
23andMers397508499
23andMe allrs397508499
SNP Nexus

SNPshotrs397508499
SNPdbers397508499
MSV3drs397508499
GWAS Ctlgrs397508499
Max Magnitude3
ClinVar
Risk rs397508499(;)
Alt rs397508499(;)
Reference rs397508499(A;A)
Significance Pathogenic
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117170989delA
CLNSRC CFTR2
CLNACC RCV000046784.3,