This variation has been flagged
Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]
Note: The reference sequence for this variant (A) does not match the Ensembl reference sequence () at this location.
Chromosome 6: between 143946045 and 143946046 (forward strand) | View in location tab
with dbSNP rs3216584 (-/G)
Archive dbSNP rs11414469
This variation has 19 HGVS names - click the plus to show