rs137852869

Orientation

plus

Stabilized

plus

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

Make rs137852869(C;C)

Make rs137852869(C;G)

Reference

GRCh38 38.1/141

Chromosome

19

Position

19516253

Gene	NDUFA13, TSSK6

is a	snp
is	mentioned by
dbSNP	rs137852869
dbSNP (classic)	rs137852869
ClinGen	rs137852869
ebi	rs137852869
HLI	rs137852869
Exac	rs137852869
Gnomad	rs137852869
Varsome	rs137852869
LitVar	rs137852869
Map	rs137852869
PheGenI	rs137852869
Biobank	rs137852869
1000 genomes	rs137852869
hgdp	rs137852869
ensembl	rs137852869
geneview	rs137852869
scholar	rs137852869
google	rs137852869
pharmgkb	rs137852869
gwascentral	rs137852869
openSNP	rs137852869
23andMe	rs137852869
SNPshot	rs137852869
SNPdbe	rs137852869
MSV3d	rs137852869
GWAS Ctlg	rs137852869

Max Magnitude

0

OMIM	609435
Desc
Variant	0001
Related	also

ClinVar
Risk	rs137852869(C;C)
Alt	rs137852869(C;C)
Reference	Rs137852869(G;G)
Significance	Pathogenic
Disease	Hurthle cell carcinoma of thyroid
Variation	info
Gene	TSSK6 NDUFA13
CLNDBN	Hurthle cell carcinoma of thyroid
Reversed	0
HGVS	NC_000019.9:g.19627062G>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000001761.3,