rs1057520786

Orientation

minus

Stabilized

minus

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

Make rs1057520786(A;A)

Make rs1057520786(A;C)

Reference

GRCh38.p7 38.3/150

Chromosome

10

Position

13281099

Gene

PHYH

is a	snp
is	mentioned by
dbSNP	rs1057520786
dbSNP (classic)	rs1057520786
ClinGen	rs1057520786
ebi	rs1057520786
HLI	rs1057520786
Exac	rs1057520786
Gnomad	rs1057520786
Varsome	rs1057520786
LitVar	rs1057520786
Map	rs1057520786
PheGenI	rs1057520786
Biobank	rs1057520786
1000 genomes	rs1057520786
hgdp	rs1057520786
ensembl	rs1057520786
geneview	rs1057520786
scholar	rs1057520786
google	rs1057520786
pharmgkb	rs1057520786
gwascentral	rs1057520786
openSNP	rs1057520786
23andMe	rs1057520786
SNPshot	rs1057520786
SNPdbe	rs1057520786
MSV3d	rs1057520786
GWAS Ctlg	rs1057520786

Max Magnitude

0

ClinVar
Risk	rs1057520786(A;A)
Alt	rs1057520786(A;A)
Reference	Rs1057520786(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	PHYH
CLNDBN	not provided
Reversed	1
HGVS	NC_000010.10:g.13323099G>T
CLNSRC
CLNACC	RCV000443182.1,