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rs876661304

From SNPedia

Orientationplus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs876661304(-;-)
Make rs876661304(-;GT)
Make rs876661304(GT;GT)
ReferenceGRCh38.p2 38.2/147
Chromosome4
Position78479678
GeneFRAS1
is asnp
is mentioned by
dbSNPrs876661304
ebirs876661304
HLIrs876661304
Exacrs876661304
Varsomers876661304
Maprs876661304
PheGenIrs876661304
hapmaprs876661304
1000 genomesrs876661304
hgdprs876661304
ensemblrs876661304
gopubmedrs876661304
geneviewrs876661304
scholarrs876661304
googlers876661304
pharmgkbrs876661304
gwascentralrs876661304
openSNPrs876661304
23andMers876661304
23andMe allrs876661304
SNP Nexus

SNPshotrs876661304
SNPdbers876661304
MSV3drs876661304
GWAS Ctlgrs876661304
Max Magnitude0
ClinVar
Risk rs876661304(;)
Alt rs876661304(;)
Reference rs876661304(TG;TG)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FRAS1
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.79400832_79400833delGT
CLNSRC
CLNACC RCV000171515.1,