rs121434590

Orientation

minus

Stabilized

minus

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

Make rs121434590(A;A)

Make rs121434590(A;G)

Reference

GRCh38 38.1/141

Chromosome

17

Position

10406924

Gene	MYH8, MYHAS

is a	snp
is	mentioned by
dbSNP	rs121434590
dbSNP (classic)	rs121434590
ClinGen	rs121434590
ebi	rs121434590
HLI	rs121434590
Exac	rs121434590
Gnomad	rs121434590
Varsome	rs121434590
LitVar	rs121434590
Map	rs121434590
PheGenI	rs121434590
Biobank	rs121434590
1000 genomes	rs121434590
hgdp	rs121434590
ensembl	rs121434590
geneview	rs121434590
scholar	rs121434590
google	rs121434590
pharmgkb	rs121434590
gwascentral	rs121434590
openSNP	rs121434590
23andMe	rs121434590
SNPshot	rs121434590
SNPdbe	rs121434590
MSV3d	rs121434590
GWAS Ctlg	rs121434590

Merged from

Rs28932773

Max Magnitude

0

OMIM	160741
Desc
Variant	0001
Related	also

ClinVar
Risk	rs121434590(A;A)
Alt	rs121434590(A;A)
Reference	Rs121434590(G;G)
Significance	Pathogenic
Disease	Carney complex variant Hecht syndrome not provided
Variation	info
Gene	MYHAS MYH8
CLNDBN	Carney complex variant Hecht syndrome not provided
Reversed	1
HGVS	NC_000017.10:g.10310241C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000015197.25, RCV000015198.25, RCV000438123.1,