rs1060502211

Orientation

plus

Stabilized

plus

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

Make rs1060502211(G;T)

Make rs1060502211(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

1

Position

156135952

Gene

LMNA

is a	snp
is	mentioned by
dbSNP	rs1060502211
dbSNP (classic)	rs1060502211
ClinGen	rs1060502211
ebi	rs1060502211
HLI	rs1060502211
Exac	rs1060502211
Gnomad	rs1060502211
Varsome	rs1060502211
LitVar	rs1060502211
Map	rs1060502211
PheGenI	rs1060502211
Biobank	rs1060502211
1000 genomes	rs1060502211
hgdp	rs1060502211
ensembl	rs1060502211
geneview	rs1060502211
scholar	rs1060502211
google	rs1060502211
pharmgkb	rs1060502211
gwascentral	rs1060502211
openSNP	rs1060502211
23andMe	rs1060502211
SNPshot	rs1060502211
SNPdbe	rs1060502211
MSV3d	rs1060502211
GWAS Ctlg	rs1060502211

Max Magnitude

0

ClinVar
Risk	rs1060502211(T;T)
Alt	rs1060502211(T;T)
Reference	Rs1060502211(G;G)
Significance	Pathogenic
Disease	Charcot-Marie-Tooth disease
Variation	info
Gene	LMNA
CLNDBN	Charcot-Marie-Tooth disease, type 2
Reversed	0
HGVS	NC_000001.10:g.156105743G>T
CLNSRC
CLNACC	RCV000467141.1,