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rs757778790

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs757778790(A;A)
Make rs757778790(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position75633674
GeneFLVCR2
is asnp
is mentioned by
dbSNPrs757778790
ebirs757778790
HLIrs757778790
Exacrs757778790
Varsomers757778790
Maprs757778790
PheGenIrs757778790
hapmaprs757778790
1000 genomesrs757778790
hgdprs757778790
ensemblrs757778790
gopubmedrs757778790
geneviewrs757778790
scholarrs757778790
googlers757778790
pharmgkbrs757778790
gwascentralrs757778790
openSNPrs757778790
23andMers757778790
23andMe allrs757778790
SNP Nexus

SNPshotrs757778790
SNPdbers757778790
MSV3drs757778790
GWAS Ctlgrs757778790
Max Magnitude0
ClinVar
Risk rs757778790(A;A)
Alt rs757778790(A;A)
Reference rs757778790(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FLVCR2
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.76100017G>A
CLNSRC
CLNACC RCV000171224.1,