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SYN2 c.774+1259T>C
Variant ID: 3-12194085-T-C
NM_133625.6(
SYN2
):c.774+1259T>C
This variant was identified in 2 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Association of TIMP4 gene variants with steroid-induced osteonecrosis of the femoral head in the population of northern China.
Peerj
Wang, Jiaqi J; An, Feimeng F; Cao, Yuju Y; Gao, Hongyan H; Sun, Mingqi M; Ma, Chao C; Wu, Hao H; Zhang, Baoxin B; Liu, Wanlin W; Wang, Jianzhong J
Publication Date: 2019
Variant appearance in text: rs99365
PubMed Link:
30697482
Variant Present in the following documents:
Main text
peerj-07-6270.pdf
View BVdb publication page
Association of synapsin 2 with schizophrenia in families of Northern European ancestry.
Schizophrenia Research
Saviouk, Viatcheslav V; Moreau, Michael P MP; Tereshchenko, Irina V IV; Brzustowicz, Linda M LM
Publication Date: 2007-11
Variant appearance in text: rs99365
PubMed Link:
17766091
Variant Present in the following documents:
Main text
View BVdb publication page