rs751161742

Orientation

plus

Stabilized

plus

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

Make rs751161742(G;G)

Make rs751161742(G;T)

Reference

GRCh38.p2 38.2/146

Chromosome

10

Position

70598384

Gene

PRF1

is a	snp
is	mentioned by
dbSNP	rs751161742
dbSNP (classic)	rs751161742
ClinGen	rs751161742
ebi	rs751161742
HLI	rs751161742
Exac	rs751161742
Gnomad	rs751161742
Varsome	rs751161742
LitVar	rs751161742
Map	rs751161742
PheGenI	rs751161742
Biobank	rs751161742
1000 genomes	rs751161742
hgdp	rs751161742
ensembl	rs751161742
geneview	rs751161742
scholar	rs751161742
google	rs751161742
pharmgkb	rs751161742
gwascentral	rs751161742
openSNP	rs751161742
23andMe	rs751161742
SNPshot	rs751161742
SNPdbe	rs751161742
MSV3d	rs751161742
GWAS Ctlg	rs751161742

Max Magnitude

0

ClinVar
Risk	rs751161742(G;G)
Alt	rs751161742(G;G)
Reference	Rs751161742(T;T)
Significance	Probable-Pathogenic
Disease	Hemophagocytic lymphohistiocytosis
Variation	info
Gene	PRF1
CLNDBN	Hemophagocytic lymphohistiocytosis, familial, 2
Reversed	0
HGVS	NC_000010.10:g.72358140T>G
CLNSRC
CLNACC	RCV000196330.1,