Total variants: 6
HGVS | dbSNP | gnomAD frequency |
---|---|---|
GRCh37/hg19 12p13. |
||
GRCh38/hg38 12p13. |
||
NM_000834. |
||
NM_000834. |
rs1057519004 | |
NM_000834. |
rs2136409494 | |
NM_000834. |
rs2136406056 |