rs1057517776

Orientation

minus

Stabilized

minus

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

Make rs1057517776(G;G)

Make rs1057517776(G;T)

Reference

GRCh38.p7 38.3/150

Chromosome

8

Position

24956222

Gene

NEFL

is a	snp
is	mentioned by
dbSNP	rs1057517776
dbSNP (classic)	rs1057517776
ClinGen	rs1057517776
ebi	rs1057517776
HLI	rs1057517776
Exac	rs1057517776
Gnomad	rs1057517776
Varsome	rs1057517776
LitVar	rs1057517776
Map	rs1057517776
PheGenI	rs1057517776
Biobank	rs1057517776
1000 genomes	rs1057517776
hgdp	rs1057517776
ensembl	rs1057517776
geneview	rs1057517776
scholar	rs1057517776
google	rs1057517776
pharmgkb	rs1057517776
gwascentral	rs1057517776
openSNP	rs1057517776
23andMe	rs1057517776
SNPshot	rs1057517776
SNPdbe	rs1057517776
MSV3d	rs1057517776
GWAS Ctlg	rs1057517776

Max Magnitude

0

ClinVar
Risk	rs1057517776(G;G)
Alt	rs1057517776(G;G)
Reference	Rs1057517776(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	NEFL
CLNDBN	not provided
Reversed	1
HGVS	NC_000008.10:g.24813736A>C
CLNSRC
CLNACC	RCV000413716.1,