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rs730881041

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730881041(A;A)
Make rs730881041(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position39023158
GeneSOS1
is asnp
is mentioned by
dbSNPrs730881041
ebirs730881041
HLIrs730881041
Exacrs730881041
Varsomers730881041
Maprs730881041
PheGenIrs730881041
hapmaprs730881041
1000 genomesrs730881041
hgdprs730881041
ensemblrs730881041
gopubmedrs730881041
geneviewrs730881041
scholarrs730881041
googlers730881041
pharmgkbrs730881041
gwascentralrs730881041
openSNPrs730881041
23andMers730881041
23andMe allrs730881041
SNP Nexus

SNPshotrs730881041
SNPdbers730881041
MSV3drs730881041
GWAS Ctlgrs730881041
Max Magnitude0
ClinVar
Risk rs730881041(A;A)
Alt rs730881041(A;A)
Reference rs730881041(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene SOS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.39250299C>T
CLNSRC
CLNACC RCV000159159.1,