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rs397508612

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GT;GT) 0 common in clinvar
Make rs397508612(-;-)
Make rs397508612(-;GT)
ReferenceGRCh38 38.1/141
Chromosome7
Position117642536
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508612
ebirs397508612
HLIrs397508612
Exacrs397508612
Varsomers397508612
Maprs397508612
PheGenIrs397508612
hapmaprs397508612
1000 genomesrs397508612
hgdprs397508612
ensemblrs397508612
gopubmedrs397508612
geneviewrs397508612
scholarrs397508612
googlers397508612
pharmgkbrs397508612
gwascentralrs397508612
openSNPrs397508612
23andMers397508612
23andMe allrs397508612
SNP Nexus

SNPshotrs397508612
SNPdbers397508612
MSV3drs397508612
GWAS Ctlgrs397508612
Max Magnitude0
ClinVar
Risk rs397508612(;)
Alt rs397508612(;)
Reference rs397508612(GT;GT)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117282590_117282591delGT
CLNSRC ClinVar
CLNACC RCV000046988.2,