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

rs77888940

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs77888940(C;G)
Make rs77888940(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome6
Position1610017
GeneFOXC1
is asnp
is mentioned by
dbSNPrs77888940
ebirs77888940
HLIrs77888940
Exacrs77888940
Varsomers77888940
Maprs77888940
PheGenIrs77888940
hapmaprs77888940
1000 genomesrs77888940
hgdprs77888940
ensemblrs77888940
gopubmedrs77888940
geneviewrs77888940
scholarrs77888940
googlers77888940
pharmgkbrs77888940
gwascentralrs77888940
openSNPrs77888940
23andMers77888940
23andMe allrs77888940
SNP Nexus

SNPshotrs77888940
SNPdbers77888940
MSV3drs77888940
GWAS Ctlgrs77888940
Max Magnitude0
ClinVar
Risk rs77888940(G;G)
Alt rs77888940(G;G)
Reference rs77888940(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene FOXC1
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.1610252C>G
CLNSRC
CLNACC RCV000162084.1,