rs876661303

Orientation

minus

Stabilized

minus

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

Make rs876661303(-;CGAGCTCCAGGCCCAGATCGC)

Make rs876661303(CGAGCTCCAGGCCCAGATCGC;CGAGCTCCAGGCCCAGATCGC)

Reference

GRCh38.p2 38.2/147

Chromosome

22

Position

36296899

Gene

MYH9

is a	snp
is	mentioned by
dbSNP	rs876661303
dbSNP (classic)	rs876661303
ClinGen	rs876661303
ebi	rs876661303
HLI	rs876661303
Exac	rs876661303
Gnomad	rs876661303
Varsome	rs876661303
LitVar	rs876661303
Map	rs876661303
PheGenI	rs876661303
Biobank	rs876661303
1000 genomes	rs876661303
hgdp	rs876661303
ensembl	rs876661303
geneview	rs876661303
scholar	rs876661303
google	rs876661303
pharmgkb	rs876661303
gwascentral	rs876661303
openSNP	rs876661303
23andMe	rs876661303
SNPshot	rs876661303
SNPdbe	rs876661303
MSV3d	rs876661303
GWAS Ctlg	rs876661303

Max Magnitude

0

ClinVar
Risk	rs876661303(CGAGCTCCAGGCCCAGATCGC;CGAGCTCCAGGCCCAGATCGC)
Alt	rs876661303(CGAGCTCCAGGCCCAGATCGC;CGAGCTCCAGGCCCAGATCGC)
Reference	Rs876661303(-;-)
Significance	Pathogenic
Disease	May-Hegglin anomaly
Variation	info
Gene	MYH9
CLNDBN	May-Hegglin anomaly
Reversed	1
HGVS	NC_000022.10:g.36692946_36692966dup21
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000015141.21,