rs786205522

Orientation

minus

Stabilized

minus

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

Make rs786205522(A;T)

Make rs786205522(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

39058794

Gene

SOS1

is a	snp
is	mentioned by
dbSNP	rs786205522
dbSNP (classic)	rs786205522
ClinGen	rs786205522
ebi	rs786205522
HLI	rs786205522
Exac	rs786205522
Gnomad	rs786205522
Varsome	rs786205522
LitVar	rs786205522
Map	rs786205522
PheGenI	rs786205522
Biobank	rs786205522
1000 genomes	rs786205522
hgdp	rs786205522
ensembl	rs786205522
geneview	rs786205522
scholar	rs786205522
google	rs786205522
pharmgkb	rs786205522
gwascentral	rs786205522
openSNP	rs786205522
23andMe	rs786205522
SNPshot	rs786205522
SNPdbe	rs786205522
MSV3d	rs786205522
GWAS Ctlg	rs786205522

Max Magnitude

0

ClinVar
Risk	rs786205522(T;T)
Alt	rs786205522(T;T)
Reference	Rs786205522(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	SOS1
CLNDBN	not provided
Reversed	1
HGVS	NC_000002.11:g.39285935T>A
CLNSRC
CLNACC	RCV000171289.1,