rs1057518337

Orientation

minus

Stabilized

minus

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

Make rs1057518337(A;G)

Make rs1057518337(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

6

Position

79042898

Gene

PHIP

is a	snp
is	mentioned by
dbSNP	rs1057518337
dbSNP (classic)	rs1057518337
ClinGen	rs1057518337
ebi	rs1057518337
HLI	rs1057518337
Exac	rs1057518337
Gnomad	rs1057518337
Varsome	rs1057518337
LitVar	rs1057518337
Map	rs1057518337
PheGenI	rs1057518337
Biobank	rs1057518337
1000 genomes	rs1057518337
hgdp	rs1057518337
ensembl	rs1057518337
geneview	rs1057518337
scholar	rs1057518337
google	rs1057518337
pharmgkb	rs1057518337
gwascentral	rs1057518337
openSNP	rs1057518337
23andMe	rs1057518337
SNPshot	rs1057518337
SNPdbe	rs1057518337
MSV3d	rs1057518337
GWAS Ctlg	rs1057518337

Max Magnitude

0

ClinVar
Risk	rs1057518337(G;G)
Alt	rs1057518337(G;G)
Reference	Rs1057518337(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	PHIP
CLNDBN	not provided
Reversed	1
HGVS	NC_000006.11:g.79752615T>C
CLNSRC
CLNACC	RCV000414004.1,