rs1060503164

Orientation

plus

Stabilized

plus

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

Make rs1060503164(A;A)

Make rs1060503164(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

117603783

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs1060503164
dbSNP (classic)	rs1060503164
ClinGen	rs1060503164
ebi	rs1060503164
HLI	rs1060503164
Exac	rs1060503164
Gnomad	rs1060503164
Varsome	rs1060503164
LitVar	rs1060503164
Map	rs1060503164
PheGenI	rs1060503164
Biobank	rs1060503164
1000 genomes	rs1060503164
hgdp	rs1060503164
ensembl	rs1060503164
geneview	rs1060503164
scholar	rs1060503164
google	rs1060503164
pharmgkb	rs1060503164
gwascentral	rs1060503164
openSNP	rs1060503164
23andMe	rs1060503164
SNPshot	rs1060503164
SNPdbe	rs1060503164
MSV3d	rs1060503164
GWAS Ctlg	rs1060503164

Max Magnitude

0

ClinVar
Risk	rs1060503164(A;A)
Alt	rs1060503164(A;A)
Reference	Rs1060503164(G;G)
Significance	Probable-Pathogenic
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117243837G>A
CLNSRC
CLNACC	RCV000465662.1,