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rs397508624

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508624(A;A)
Make rs397508624(A;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117652841
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508624
ebirs397508624
HLIrs397508624
Exacrs397508624
Varsomers397508624
Maprs397508624
PheGenIrs397508624
hapmaprs397508624
1000 genomesrs397508624
hgdprs397508624
ensemblrs397508624
gopubmedrs397508624
geneviewrs397508624
scholarrs397508624
googlers397508624
pharmgkbrs397508624
gwascentralrs397508624
openSNPrs397508624
23andMers397508624
23andMe allrs397508624
SNP Nexus

SNPshotrs397508624
SNPdbers397508624
MSV3drs397508624
GWAS Ctlgrs397508624
Max Magnitude0
ClinVar
Risk rs397508624(A;A)
Alt rs397508624(A;A)
Reference rs397508624(G;G)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117292895G>A
CLNSRC ClinVar
CLNACC RCV000047009.2,