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
with dbSNP rs375394098 (-/A)
Archive dbSNP rs59806607
This variation has 31 HGVS names - click the plus to show
This variant overlaps 32 transcripts.