rs1057518206

Orientation

plus

Stabilized

plus

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

Make rs1057518206(A;G)

Make rs1057518206(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

10

Position

110964875

Gene

SHOC2

is a	snp
is	mentioned by
dbSNP	rs1057518206
dbSNP (classic)	rs1057518206
ClinGen	rs1057518206
ebi	rs1057518206
HLI	rs1057518206
Exac	rs1057518206
Gnomad	rs1057518206
Varsome	rs1057518206
LitVar	rs1057518206
Map	rs1057518206
PheGenI	rs1057518206
Biobank	rs1057518206
1000 genomes	rs1057518206
hgdp	rs1057518206
ensembl	rs1057518206
geneview	rs1057518206
scholar	rs1057518206
google	rs1057518206
pharmgkb	rs1057518206
gwascentral	rs1057518206
openSNP	rs1057518206
23andMe	rs1057518206
SNPshot	rs1057518206
SNPdbe	rs1057518206
MSV3d	rs1057518206
GWAS Ctlg	rs1057518206

Max Magnitude

0

ClinVar
Risk	rs1057518206(G;G)
Alt	rs1057518206(G;G)
Reference	Rs1057518206(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	SHOC2
CLNDBN	not provided
Reversed	0
HGVS	NC_000010.10:g.112724633A>G
CLNSRC
CLNACC	RCV000413825.1,