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rs371940910

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs371940910(A;G)
Make rs371940910(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome15
Position34792142
GeneACTC1, LOC101928174
is asnp
is mentioned by
dbSNPrs371940910
ebirs371940910
HLIrs371940910
Exacrs371940910
Varsomers371940910
Maprs371940910
PheGenIrs371940910
hapmaprs371940910
1000 genomesrs371940910
hgdprs371940910
ensemblrs371940910
gopubmedrs371940910
geneviewrs371940910
scholarrs371940910
googlers371940910
pharmgkbrs371940910
gwascentralrs371940910
openSNPrs371940910
23andMers371940910
23andMe allrs371940910
SNP Nexus

SNPshotrs371940910
SNPdbers371940910
MSV3drs371940910
GWAS Ctlgrs371940910
Max Magnitude0
ClinVar
Risk rs371940910(C,G;C,G)
Alt rs371940910(C,G;C,G)
Reference rs371940910(A;A)
Significance Pathogenic
Disease not specified
Variation info
Gene ACTC1 LOC101928174 RP11-814P5.1
CLNDBN not specified
Reversed 0
HGVS NC_000015.9:g.35084343A>C
CLNSRC
CLNACC RCV000150128.2,