rs1060500344

Orientation

plus

Stabilized

plus

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

Make rs1060500344(A;T)

Make rs1060500344(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

17

Position

31338138

Gene

NF1

is a	snp
is	mentioned by
dbSNP	rs1060500344
dbSNP (classic)	rs1060500344
ClinGen	rs1060500344
ebi	rs1060500344
HLI	rs1060500344
Exac	rs1060500344
Gnomad	rs1060500344
Varsome	rs1060500344
LitVar	rs1060500344
Map	rs1060500344
PheGenI	rs1060500344
Biobank	rs1060500344
1000 genomes	rs1060500344
hgdp	rs1060500344
ensembl	rs1060500344
geneview	rs1060500344
scholar	rs1060500344
google	rs1060500344
pharmgkb	rs1060500344
gwascentral	rs1060500344
openSNP	rs1060500344
23andMe	rs1060500344
SNPshot	rs1060500344
SNPdbe	rs1060500344
MSV3d	rs1060500344
GWAS Ctlg	rs1060500344

Max Magnitude

0

ClinVar
Risk	rs1060500344(T;T)
Alt	rs1060500344(T;T)
Reference	Rs1060500344(A;A)
Significance	Probable-Pathogenic
Disease	Hereditary cancer-predisposing syndrome Neurofibromatosis
Variation	info
Gene	NF1
CLNDBN	Hereditary cancer-predisposing syndrome Neurofibromatosis, type 1
Reversed	0
HGVS	NC_000017.10:g.29665156A>G; NC_000017.10:g.29665156A>T
CLNSRC
CLNACC	RCV000492274.1, RCV000463991.1,