Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

Alleles
A/C | Ancestral: A | Ambiguity code: M | MAF: 0.22 (C)
Location

Chromosome 10:100193948 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs17880376, rs56743359

This variation has 4 HGVS names - click the plus to show

10:g.100193948A>C
ENST00000588656.1:n.96+36T>G
ENST00000590930.2:n.1995T>G
ENST00000370397.7:c.1974+36T>G

This variation has assays on 7 chips - click the plus to show

Variation displays