rs1057523861

Orientation

plus

Stabilized

plus

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

Make rs1057523861(A;A)

Make rs1057523861(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

12

Position

32710995

Gene

DNM1L

is a	snp
is	mentioned by
dbSNP	rs1057523861
dbSNP (classic)	rs1057523861
ClinGen	rs1057523861
ebi	rs1057523861
HLI	rs1057523861
Exac	rs1057523861
Gnomad	rs1057523861
Varsome	rs1057523861
LitVar	rs1057523861
Map	rs1057523861
PheGenI	rs1057523861
Biobank	rs1057523861
1000 genomes	rs1057523861
hgdp	rs1057523861
ensembl	rs1057523861
geneview	rs1057523861
scholar	rs1057523861
google	rs1057523861
pharmgkb	rs1057523861
gwascentral	rs1057523861
openSNP	rs1057523861
23andMe	rs1057523861
SNPshot	rs1057523861
SNPdbe	rs1057523861
MSV3d	rs1057523861
GWAS Ctlg	rs1057523861

Max Magnitude

0

ClinVar
Risk	rs1057523861(A;A)
Alt	rs1057523861(A;A)
Reference	Rs1057523861(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	DNM1L
CLNDBN	not provided
Reversed	0
HGVS	NC_000012.11:g.32863929G>A
CLNSRC
CLNACC	RCV000443148.1,