rs587777926

Merged into

rs397508163

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;-)	0	common in clinvar

Make rs587777926(-;A)

Make rs587777926(A;A)

Reference

GRCh38.p2 38.2/144

Chromosome

7

Position

117542027

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs587777926
dbSNP (classic)	rs587777926
ClinGen	rs587777926
ebi	rs587777926
HLI	rs587777926
Exac	rs587777926
Gnomad	rs587777926
Varsome	rs587777926
LitVar	rs587777926
Map	rs587777926
PheGenI	rs587777926
Biobank	rs587777926
1000 genomes	rs587777926
hgdp	rs587777926
ensembl	rs587777926
geneview	rs587777926
scholar	rs587777926
google	rs587777926
pharmgkb	rs587777926
gwascentral	rs587777926
openSNP	rs587777926
23andMe	rs587777926
SNPshot	rs587777926
SNPdbe	rs587777926
MSV3d	rs587777926
GWAS Ctlg	rs587777926

Status

Merged into rs397508163

Max Magnitude

0

ClinVar
Risk	rs587777926(A;A)
Alt	rs587777926(A;A)
Reference	Rs587777926(;)
Significance	Pathogenic
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117182081dupA
CLNSRC	CFTR2
CLNACC	RCV000056341.3,