rs267606610

Orientation

plus

Stabilized

plus

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

Make rs267606610(A;C)

Make rs267606610(C;C)

Reference

GRCh38 38.1/141

Chromosome

17

Position

31343138

Gene

NF1

is a	snp
is	mentioned by
dbSNP	rs267606610
dbSNP (classic)	rs267606610
ClinGen	rs267606610
ebi	rs267606610
HLI	rs267606610
Exac	rs267606610
Gnomad	rs267606610
Varsome	rs267606610
LitVar	rs267606610
Map	rs267606610
PheGenI	rs267606610
Biobank	rs267606610
1000 genomes	rs267606610
hgdp	rs267606610
ensembl	rs267606610
geneview	rs267606610
scholar	rs267606610
google	rs267606610
pharmgkb	rs267606610
gwascentral	rs267606610
openSNP	rs267606610
23andMe	rs267606610
SNPshot	rs267606610
SNPdbe	rs267606610
MSV3d	rs267606610
GWAS Ctlg	rs267606610

Max Magnitude

0

ClinVar
Risk	rs267606610(C;C)
Alt	rs267606610(C;C)
Reference	Rs267606610(A;A)
Significance	Pathogenic
Disease	Neurofibromatosis
Variation	info
Gene	NF1
CLNDBN	Neurofibromatosis, familial spinal
Reversed	0
HGVS	NC_000017.10:g.29670156A>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000000400.4,