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 10: between 112956367 and 112956368 (forward strand) | View in location tab
Archive dbSNP rs59806607
This variation has 27 HGVS names - click the plus to show