rs797045157

Merged into

rs387906359

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(;)	0	common in clinvar
(-;-)	0	common/normal
(-;AT)	3	carrier of a cystic fibrosis allele

Make rs797045157(AT;AT)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

117592591

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs797045157
dbSNP (classic)	rs797045157
ClinGen	rs797045157
ebi	rs797045157
HLI	rs797045157
Exac	rs797045157
Gnomad	rs797045157
Varsome	rs797045157
LitVar	rs797045157
Map	rs797045157
PheGenI	rs797045157
Biobank	rs797045157
1000 genomes	rs797045157
hgdp	rs797045157
ensembl	rs797045157
geneview	rs797045157
scholar	rs797045157
google	rs797045157
pharmgkb	rs797045157
gwascentral	rs797045157
openSNP	rs797045157
23andMe	rs797045157
SNPshot	rs797045157
SNPdbe	rs797045157
MSV3d	rs797045157
GWAS Ctlg	rs797045157

Status

Merged into rs387906359

Max Magnitude

3

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,