rs199474665

Orientation

plus

Stabilized

plus

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

Make rs199474665(C;C)

Make rs199474665(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

MT

Position

3290

is a	snp
is	mentioned by
dbSNP	rs199474665
dbSNP (classic)	rs199474665
ClinGen	rs199474665
ebi	rs199474665
HLI	rs199474665
Exac	rs199474665
Gnomad	rs199474665
Varsome	rs199474665
LitVar	rs199474665
Map	rs199474665
PheGenI	rs199474665
Biobank	rs199474665
1000 genomes	rs199474665
hgdp	rs199474665
ensembl	rs199474665
geneview	rs199474665
scholar	rs199474665
google	rs199474665
pharmgkb	rs199474665
gwascentral	rs199474665
openSNP	rs199474665
23andMe	rs199474665
SNPshot	rs199474665
SNPdbe	rs199474665
MSV3d	rs199474665
GWAS Ctlg	rs199474665

GMAF

0.001871

Max Magnitude

0

ClinVar
Risk	rs199474665(C;C)
Alt	rs199474665(C;C)
Reference	Rs199474665(T;T)
Significance	Pathogenic
Disease	SUDDEN INFANT DEATH SYNDROME
Variation	info
Gene
CLNDBN	SUDDEN INFANT DEATH SYNDROME
Reversed	0
HGVS	NC_012920.1:m.3290T>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010220.2,