rs2075507
变体ID
PA166156085
基因 ID
PA117,PA38302
基因符号
COMT,TXNRD2
位置
NC_000022.11:19940569
变异注释计数
1
临床注释计数
0
1-2级临床注释计数
0
指南注释计数
0
标签注释计数
0
同义词
2097603, NG_011835.1:g.6268C>A, rs2097603, 2234763, rs2234763, XM_011529890.1:c.-1714G>A, NG_011526.1:g.3830G>T, NC_000022.11:g.19940569G>T, NG_011835.1:g.6268=, XM_005261216.1:c.103+1132C>T, NC_000022.10:g.19928092G>A, XM_011529891.1:c.-1992G>A, rs4646309, NC_000022.10:g.19928092G>C, NM_006440.4:c.103+1132C>T, NC_000022.11:g.19940569G>A, NC_000022.10:g.19928092=, NC_000022.11:g.19940569G>C, rs2075507, 2075507, NC_000022.11:g.19940569=, 3937420, NM_000754.3:c.-1420G>A, XM_005261214.1:c.103+1132C>T, XM_011529887.1:c.-1420G>A, NC_000022.10:g.19928092G>T, XM_005261217.1:c.103+1132C>T, 4646309, rs3937420, NG_011526.1:g.3830G>A, NG_011526.1:g.3830G>C, NG_011526.1:g.3830=, NM_006440.3:c.103+1132C>T, NG_011835.1:g.6268C>T, NG_011835.1:g.6268C>G, NM_001282512.1:c.103+1132C>T, XM_005261229.1:c.-1714G>A

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