rs193303018

Orientation

plus

Stabilized

plus

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

Make rs193303018(A;A)

Make rs193303018(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

MT

Position

3242

is a	snp
is	mentioned by
dbSNP	rs193303018
dbSNP (classic)	rs193303018
ClinGen	rs193303018
ebi	rs193303018
HLI	rs193303018
Exac	rs193303018
Gnomad	rs193303018
Varsome	rs193303018
LitVar	rs193303018
Map	rs193303018
PheGenI	rs193303018
Biobank	rs193303018
1000 genomes	rs193303018
hgdp	rs193303018
ensembl	rs193303018
geneview	rs193303018
scholar	rs193303018
google	rs193303018
pharmgkb	rs193303018
gwascentral	rs193303018
openSNP	rs193303018
23andMe	rs193303018
SNPshot	rs193303018
SNPdbe	rs193303018
MSV3d	rs193303018
GWAS Ctlg	rs193303018

Merged from

Rs199474668

Max Magnitude

0

ClinVar
Risk	rs193303018(A;A)
Alt	rs193303018(A;A)
Reference	Rs193303018(G;G)
Significance	Pathogenic
Disease	Myelodysplastic syndrome
Variation	info
Gene
CLNDBN	Myelodysplastic syndrome
Reversed	0
HGVS	NC_012920.1:m.3242G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010223.6,