rs1057517276

Orientation

plus

Stabilized

plus

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

Make rs1057517276(-;A)

Make rs1057517276(A;A)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

117592650

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs1057517276
dbSNP (classic)	rs1057517276
ClinGen	rs1057517276
ebi	rs1057517276
HLI	rs1057517276
Exac	rs1057517276
Gnomad	rs1057517276
Varsome	rs1057517276
LitVar	rs1057517276
Map	rs1057517276
PheGenI	rs1057517276
Biobank	rs1057517276
1000 genomes	rs1057517276
hgdp	rs1057517276
ensembl	rs1057517276
geneview	rs1057517276
scholar	rs1057517276
google	rs1057517276
pharmgkb	rs1057517276
gwascentral	rs1057517276
openSNP	rs1057517276
23andMe	rs1057517276
SNPshot	rs1057517276
SNPdbe	rs1057517276
MSV3d	rs1057517276
GWAS Ctlg	rs1057517276

Max Magnitude

0

ClinVar
Risk	rs1057517276(A;A)
Alt	rs1057517276(A;A)
Reference	Rs1057517276(-;-)
Significance	Probable-Pathogenic
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117232704dupA
CLNSRC
CLNACC	RCV000410112.1,