ClinVar Miner

List of variants in gene KCNQ2 reported as benign for not provided

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Total variants: 31
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HGVS dbSNP
GRCh37/hg19 20q13.33(chr20:62075098-62119121)x4
NC_000020.11:g.63413761_63413762del
NC_000020.11:g.63419886dup
NM_172107.4(KCNQ2):c.1024-164G>A
NM_172107.4(KCNQ2):c.1024-204C>T
NM_172107.4(KCNQ2):c.1148+117C>T
NM_172107.4(KCNQ2):c.1217+215C>T
NM_172107.4(KCNQ2):c.1217+298C>T
NM_172107.4(KCNQ2):c.1218-180G>A
NM_172107.4(KCNQ2):c.1247+113C>T
NM_172107.4(KCNQ2):c.1302-275_1302-274insT
NM_172107.4(KCNQ2):c.1526-163G>A
NM_172107.4(KCNQ2):c.1631+141C>T
NM_172107.4(KCNQ2):c.1764-133A>G
NM_172107.4(KCNQ2):c.1764-283C>T
NM_172107.4(KCNQ2):c.1887+150T>C
NM_172107.4(KCNQ2):c.1888-138C>G
NM_172107.4(KCNQ2):c.1888-195C>G
NM_172107.4(KCNQ2):c.1888-82C>G
NM_172107.4(KCNQ2):c.297-297A>G
NM_172107.4(KCNQ2):c.388-26G>T
NM_172107.4(KCNQ2):c.388-271A>G
NM_172107.4(KCNQ2):c.388-285T>G
NM_172107.4(KCNQ2):c.388-296_388-295dup
NM_172107.4(KCNQ2):c.388-298G>C
NM_172107.4(KCNQ2):c.388-303G>C
NM_172107.4(KCNQ2):c.388-319del
NM_172107.4(KCNQ2):c.388-325A>T
NM_172107.4(KCNQ2):c.515-76C>T
NM_172107.4(KCNQ2):c.928-228G>A
NM_172107.4(KCNQ2):c.928-87G>C

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