S100B, S100 calcium binding protein B, 6285

N. diseases: 599; N. variants: 6
Disease: MAJOR AFFECTIVE DISORDER 4 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3788266
rs3788266
Entrez Id: 6285
Gene Symbol: S100B
S100B
CUI: C1970943
Disease:
MAJOR AFFECTIVE DISORDER 4 		0.020 GeneticVariation BEFREE Higher mean serum S100B levels were associated with the risk G allele of rs3788266 in BPAD cases (P = 0.0001), unaffected relatives of BPAD cases (P < 0.0001) and unrelated controls (P < 0.0001). 21714070 2011
dbSNP: rs3788266
rs3788266
Entrez Id: 6285
Gene Symbol: S100B
S100B
CUI: C1970943
Disease:
MAJOR AFFECTIVE DISORDER 4 		0.020 GeneticVariation BEFREE S100B single nucleotide polymorphisms (SNPs) rs2839350 (P = 0.022) and rs3788266 (P = 0.031) were significantly associated with BPAD. 17525977 2007