rs1060500292

Orientation

plus

Stabilized

plus

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

Make rs1060500292(-;-)

Make rs1060500292(-;G)

Reference

GRCh38.p7 38.3/150

Chromosome

17

Position

31261731

Gene

NF1

is a	snp
is	mentioned by
dbSNP	rs1060500292
dbSNP (classic)	rs1060500292
ClinGen	rs1060500292
ebi	rs1060500292
HLI	rs1060500292
Exac	rs1060500292
Gnomad	rs1060500292
Varsome	rs1060500292
LitVar	rs1060500292
Map	rs1060500292
PheGenI	rs1060500292
Biobank	rs1060500292
1000 genomes	rs1060500292
hgdp	rs1060500292
ensembl	rs1060500292
geneview	rs1060500292
scholar	rs1060500292
google	rs1060500292
pharmgkb	rs1060500292
gwascentral	rs1060500292
openSNP	rs1060500292
23andMe	rs1060500292
SNPshot	rs1060500292
SNPdbe	rs1060500292
MSV3d	rs1060500292
GWAS Ctlg	rs1060500292

Max Magnitude

0

ClinVar
Risk	rs1060500292(-;-)
Alt	rs1060500292(-;-)
Reference	Rs1060500292(G;G)
Significance	Pathogenic
Disease	Neurofibromatosis
Variation	info
Gene	NF1
CLNDBN	Neurofibromatosis, type 1
Reversed	0
HGVS	NC_000017.10:g.29588749delG
CLNSRC
CLNACC	RCV000474271.1,