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rs786205570

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786205570(A;A)
Make rs786205570(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position78478063
GeneFRAS1
is asnp
is mentioned by
dbSNPrs786205570
ebirs786205570
HLIrs786205570
Exacrs786205570
Varsomers786205570
Maprs786205570
PheGenIrs786205570
hapmaprs786205570
1000 genomesrs786205570
hgdprs786205570
ensemblrs786205570
gopubmedrs786205570
geneviewrs786205570
scholarrs786205570
googlers786205570
pharmgkbrs786205570
gwascentralrs786205570
openSNPrs786205570
23andMers786205570
23andMe allrs786205570
SNP Nexus

SNPshotrs786205570
SNPdbers786205570
MSV3drs786205570
GWAS Ctlgrs786205570
Max Magnitude0
ClinVar
Risk rs786205570(A;A)
Alt rs786205570(A;A)
Reference rs786205570(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FRAS1
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.79399217T>A
CLNSRC
CLNACC RCV000171378.1,