Have questions? Visit https://www.reddit.com/r/SNPedia

rs730881010

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730881010(A;T)
Make rs730881010(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position12604185
GeneRAF1
is asnp
is mentioned by
dbSNPrs730881010
ebirs730881010
HLIrs730881010
Exacrs730881010
Varsomers730881010
Maprs730881010
PheGenIrs730881010
hapmaprs730881010
1000 genomesrs730881010
hgdprs730881010
ensemblrs730881010
gopubmedrs730881010
geneviewrs730881010
scholarrs730881010
googlers730881010
pharmgkbrs730881010
gwascentralrs730881010
openSNPrs730881010
23andMers730881010
23andMe allrs730881010
SNP Nexus

SNPshotrs730881010
SNPdbers730881010
MSV3drs730881010
GWAS Ctlgrs730881010
Max Magnitude0
ClinVar
Risk rs730881010(T;T)
Alt rs730881010(T;T)
Reference rs730881010(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene RAF1
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.12645684T>A
CLNSRC
CLNACC RCV000159095.1,