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rs1057521631

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057521631(A;T)
Make rs1057521631(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position52464921
GeneEFHC1
is asnp
is mentioned by
dbSNPrs1057521631
dbSNP (old)rs1057521631
ClinGenrs1057521631
ebirs1057521631
HLIrs1057521631
Exacrs1057521631
Gnomadrs1057521631
Varsomers1057521631
Maprs1057521631
PheGenIrs1057521631
Biobankrs1057521631
1000 genomesrs1057521631
hgdprs1057521631
ensemblrs1057521631
gopubmedrs1057521631
geneviewrs1057521631
scholarrs1057521631
googlers1057521631
pharmgkbrs1057521631
gwascentralrs1057521631
openSNPrs1057521631
23andMers1057521631
23andMe allrs1057521631
SNPshotrs1057521631
SNPdbers1057521631
MSV3drs1057521631
GWAS Ctlgrs1057521631
Max Magnitude0
ClinVar
Risk rs1057521631(T;T)
Alt rs1057521631(T;T)
Reference Rs1057521631(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene EFHC1
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.52329719A>T
CLNSRC
CLNACC RCV000431419.1,