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rs797045157

From SNPedia

Merged intors387906359
Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
(-;-) 0 common/normal
(-;AT) 3 carrier of a cystic fibrosis allele
Make rs797045157(AT;AT)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position117592591
GeneCFTR
is asnp
is mentioned by
dbSNPrs797045157
dbSNP (old)rs797045157
ClinGenrs797045157
ebirs797045157
HLIrs797045157
Exacrs797045157
Gnomadrs797045157
Varsomers797045157
Maprs797045157
PheGenIrs797045157
Biobankrs797045157
1000 genomesrs797045157
hgdprs797045157
ensemblrs797045157
gopubmedrs797045157
geneviewrs797045157
scholarrs797045157
googlers797045157
pharmgkbrs797045157
gwascentralrs797045157
openSNPrs797045157
23andMers797045157
23andMe allrs797045157
SNP Nexus

SNPshotrs797045157
SNPdbers797045157
MSV3drs797045157
GWAS Ctlgrs797045157
StatusMerged into rs387906359
Max Magnitude3
ClinVar
Risk rs797045157(AT;AT)
Alt rs797045157(AT;AT)
Reference Rs797045157(;)
Significance Pathogenic
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117232644_117232645dupAT
CLNSRC CFTR2 OMIM Allelic Variant
CLNACC RCV000190991.2,