rs387906860

Orientation

minus

Stabilized

minus

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

Make rs387906860(-;C)

Make rs387906860(C;C)

Reference

GRCh38 38.1/141

Chromosome

16

Position

16219577

Gene

ABCC6

is a	snp
is	mentioned by
dbSNP	rs387906860
dbSNP (classic)	rs387906860
ClinGen	rs387906860
ebi	rs387906860
HLI	rs387906860
Exac	rs387906860
Gnomad	rs387906860
Varsome	rs387906860
LitVar	rs387906860
Map	rs387906860
PheGenI	rs387906860
Biobank	rs387906860
1000 genomes	rs387906860
hgdp	rs387906860
ensembl	rs387906860
geneview	rs387906860
scholar	rs387906860
google	rs387906860
pharmgkb	rs387906860
gwascentral	rs387906860
openSNP	rs387906860
23andMe	rs387906860
SNPshot	rs387906860
SNPdbe	rs387906860
MSV3d	rs387906860
GWAS Ctlg	rs387906860

Max Magnitude

0

ClinVar
Risk	rs387906860(C;C)
Alt	rs387906860(C;C)
Reference	Rs387906860(-;-)
Significance	Pathogenic
Disease	Generalized arterial calcification of infancy 2
Variation	info
Gene	ABCC6
CLNDBN	Generalized arterial calcification of infancy 2
Reversed	1
HGVS	NC_000016.9:g.16313435dupG
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000023281.3,