rs199474668

Merged into

rs193303018

Orientation

plus

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

Make rs199474668(A;A)

Make rs199474668(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

MT

Position

3242

is a	snp
is	mentioned by
dbSNP	rs199474668
dbSNP (classic)	rs199474668
ClinGen	rs199474668
ebi	rs199474668
HLI	rs199474668
Exac	rs199474668
Gnomad	rs199474668
Varsome	rs199474668
LitVar	rs199474668
Map	rs199474668
PheGenI	rs199474668
Biobank	rs199474668
1000 genomes	rs199474668
hgdp	rs199474668
ensembl	rs199474668
geneview	rs199474668
scholar	rs199474668
google	rs199474668
pharmgkb	rs199474668
gwascentral	rs199474668
openSNP	rs199474668
23andMe	rs199474668
SNPshot	rs199474668
SNPdbe	rs199474668
MSV3d	rs199474668
GWAS Ctlg	rs199474668

Status

Merged into rs193303018

Max Magnitude

0

ClinVar
Risk	rs199474668(A;A)
Alt	rs199474668(A;A)
Reference	Rs199474668(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	RCV000010223.4,