rs864309486

Orientation

plus

Stabilized

plus

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

Make rs864309486(A;T)

Make rs864309486(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

6

Position

24777262

Gene

GMNN

is a	snp
is	mentioned by
dbSNP	rs864309486
dbSNP (classic)	rs864309486
ClinGen	rs864309486
ebi	rs864309486
HLI	rs864309486
Exac	rs864309486
Gnomad	rs864309486
Varsome	rs864309486
LitVar	rs864309486
Map	rs864309486
PheGenI	rs864309486
Biobank	rs864309486
1000 genomes	rs864309486
hgdp	rs864309486
ensembl	rs864309486
geneview	rs864309486
scholar	rs864309486
google	rs864309486
pharmgkb	rs864309486
gwascentral	rs864309486
openSNP	rs864309486
23andMe	rs864309486
SNPshot	rs864309486
SNPdbe	rs864309486
MSV3d	rs864309486
GWAS Ctlg	rs864309486

Max Magnitude

0

ClinVar
Risk	rs864309486(T;T)
Alt	rs864309486(T;T)
Reference	Rs864309486(A;A)
Significance	Pathogenic
Disease	Meier-Gorlin syndrome Meier-gorlin syndrome 6
Variation	info
Gene	GMNN
CLNDBN	Meier-Gorlin syndrome Meier-gorlin syndrome 6
Reversed	0
HGVS	NC_000006.11:g.24777490A>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000202433.1, RCV000208589.1,