Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome 1:97564154 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM973073

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

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

1:g.97564154C>T
ENST00000422980.1:n.64+2612C>T
ENST00000370192.3:c.2657G>A
ENSP00000359211.3:p.Arg886His

Genotyping chips

This variation has assays on: Illumina_1M-duo, Illumina_ExomeChip, Illumina_HumanOmni1-Quad

Variation displays